Heterocyclic substituted pyridine or phenyl compounds with CXCR3 antagonist activity

ABSTRACT

The present application discloses a compound, or enantiomers, stereoisomers, rotamers, tautomers, racemates or prodrug of said compound, or pharmaceutically acceptable salts, solvates or esters of said compound, or of said prodrug, said compound having the general structure shown in Formula 1: 
                         
or a pharmaceutically acceptable salt, solvate or ester thereof. Also disclosed is a method of treating chemokine mediated diseases, such as, palliative therapy, curative therapy, prophylactic therapy of certain diseases and conditions such as inflammatory diseases (non-limiting example(s) include, psoriasis), autoimmune diseases (non-limiting example(s) include, rheumatoid arthritis, multiple sclerosis), graft rejection (non-limiting example(s) include, allograft rejection, zenograft rejection), infectious diseases (e.g, tuberculoid leprosy), fixed drug eruptions, cutaneous delayed-type hypersensitivity responses, ophthalmic inflammation, type I diabetes, viral meningitis and tumors using a compound of Formula 1.

This application is a divisional of U.S. application Ser. No. 11/353,609filed Feb. 14, 2006, which claims the benefit of U.S. provisionalapplication Ser. No. 60/653,332 filed Feb. 16, 2005.

FIELD OF THE INVENTION

The present invention relates to novel heterocyclic substitutedpiperazines with CXCR3 antagonist activity, pharmaceutical compositionscontaining one or more such antagonists, one or more such antagonists incombination with other compounds with chemokine activity, one or moresuch antagonists in combination with known immunosuppressive agents,non-limiting example(s) include Methotrexate, interferon, cyclosporin,FK-506 and FTY720, methods of preparing such antagonists and methods ofusing such antagonists to modulate CXCR3 activity. This invention alsodiscloses methods of using such CXCR3 antagonists for the treatment(non-limiting examples include palliative, curative and prophylactictherapies) of diseases and conditions where CXCR3 has been implicated.Diseases and conditions where CXCR3 has been implicated include but arenot limited to inflammatory conditions (psoriasis and inflammatory boweldisease), autoimmune disease (multiple sclerosis, rheumatoid arthritis),fixed drug eruptions, cutaneous delayed-type hypersensitivity responses,type I diabetes, viral meningitis and tuberculoid leprosy. CXCR3antagonist activity has also been indicated as a therapy for tumorgrowth suppression as well as graft rejection (allograft and zenograftrejections for example).

BACKGROUND OF THE INVENTION

Chemokines constitute a family of cytokines that are produced ininflammation and regulate leukocyte recruitment (Baggiolini, M. et al.,Adv. Immunol., 55: 97-179 (1994); Springer, T. A., Annual Rev. Physio.,57: 827-872 (1995); and Schall, T. J. and K. B. Bacon, Curr. Opin.Immunol, 6: 865-873 (1994)). Chemokines are capable of selectivelyinducing chemotaxis of the formed elements of the blood (other than redblood cells), including leukocytes such as neutrophils, monocytes,macrophages, eosinophils, basophils, mast cells, and lymphocytes, suchas T cells and B cells. In addition to stimulating chemotaxis, otherchanges can be selectively induced by chemokines in responsive cells,including changes in cell shape, transient rises in the concentration ofintracellular free calcium ions ([Ca²⁺]_(i)), granule exocytosis,integrin upregulation, formation of bioactive lipids (e.g.,leukotrienes) and respiratory burst, associated with leukocyteactivation. Thus, the chemokines are early triggers of the inflammatoryresponse, causing inflammatory mediator release, chemotaxis andextravasation to sites of infection or inflammation.

Chemokines are related in primary structure and share four conservedcysteines, which form disulfide bonds. Based upon this conservedcysteine motif, the family can be divided into distinct branches,including the C—X—C chemokines (α-chemokines) in which the first twoconserved cysteines are separated by an intervening residue (e.g., IL-8,IP-10, Mig, I-TAC, PF4, ENA-78, GCP-2, GROα, GROβ, GROδ, NAP-2, NAP-4),and the C—C chemokines (β-chemokines), in which the first two conservedcysteines are adjacent residues (e.g., MIP-1α, MIP-1β, RANTES, MCP-1,MCP-2, MCP-3, 1-309) (Baggiolini, M. and Dahinden, C. A., ImmunologyToday, 15: 127-133 (1994)). Most CXC-chemokines attract neutrophilleukocytes. For example, the CXC-chemokines interleukin-8 (IL-8), GROalpha (GROα), and neutrophil-activating peptide 2 (NAP-2) are potentchemoattractants and activators of neutrophils. The CXC-chemokinesdesignated Mig (monokine induced by gamma interferon) and IP-10(interferon-gamma inducible 10 kDa protein) are particularly active ininducing chemotaxis of activated peripheral blood lymphocytes.

CC-chemokines are generally less selective and can attract a variety ofleukocyte cell types, including monocytes, eosinophils, basophils, Tlymphocytes and natural killer cells. CC-chemokines such as humanmonocyte chemotactic proteins 1-3 (MCP-1, MCP-2 and MCP-3), RANTES(Regulated on Activation, Normal T Expressed and Secreted), and themacrophage inflammatory proteins 1α and 1β (MIP-1α and MIP-1β) have beencharacterized as chemoattractants and activators of monocytes orlymphocytes, but do not appear to be chemoattractants for neutrophils.

A chemokine receptor that binds the CXC-chemokines IP-10 and Mig hasbeen cloned, characterized (Loetscher, M. et al., J. Exp. Med., 184:963-969 (1996)) and designated CXCR3. CXCR3 is a G-protein coupledreceptor with seven transmembrane-spanning domains and has been shown tobe restrictively expressed in activated T cells, preferentially humanTh1 cells. On binding of the appropriate ligand, chemokine receptorstransduce an intracellular signal through the associated G-proteinresulting in a rapid increase in intracellular calcium concentration.

The CXCR3 receptor mediates Ca²⁺ (calcium ion) mobilization andchemotaxis in response to IP-10 and Mig. CXCR3 expressing cells show nosignificant response to the CXC-chemokines IL-8, GROα, NAP-2, GCP-2(granulocyte chemotactic protein-2), ENA78 (epithelial-derivedneutrophil-activating peptide 78), PF4 (platelet factor 4), or theCC-chemokines MCP-1, MCP-2, MCP-3, MCP-4, MIP-1α, MIP-1β, RANTES, I309,eotaxin or lymphotactin. Moreover, a third ligand for CXCR3, I-TAC(Interferon-inducible T cell Alpha Chemoattractant), has also been foundto bind to the receptor with high affinity and mediate functionalresponses (Cole, K. E. et al., J. Exp. Med., 187: 2009-2021 (1998)).

The restricted expression of human CXCR3 in activated T lymphocytes andthe ligand selectivity of CXCR3 are noteworthy. The human receptor ishighly expressed in IL-2 activated T lymphocytes, but was not detectedin resting T lymphocytes, monocytes or granulocytes (Qin, S. et al., J.Clin. Invest., 101: 746-754 (1998)). Additional studies of receptordistribution indicate that it is mostly CD3⁺ cells that express CXCR3,including cells which are CD95⁺, CD45RO⁺, and CD45RA^(low), a phenotypeconsistent with previous activation, although a proportion of CD20⁺ (B)cells and CD56⁺ (NK) cells also express this receptor. The selectiveexpression in activated T lymphocytes is of interest, because otherreceptors for chemokines which have been reported to attract lymphocytes(e.g., MCP-1, MCP-2, MCP-3, MIP-1α, MIP-1β, RANTES) are also expressedby granulocytes, such as neutrophils, eosinophils, and basophils, aswell as monocytes. These results suggest that the CXCR3 receptor isinvolved in the selective recruitment of effector T cells.

CXCR3 recognizes unusual CXC-chemokines, designated IP-10, Mig andI-TAC. Although these belong to the CXC-subfamily, in contrast to IL-8and other CXC-chemokines which are potent chemoattractants forneutrophils, the primary targets of IP-10, Mig and I-TAC arelymphocytes, particularly effector cells such as activated or stimulatedT lymphocytes and natural killer (NK) cells (Taub, D. D. et al., J. Exp.Med., 177: 18090-1814 (1993); Taub, D. D. et al., J. Immunol., 155:3877-3888 (1995); Cole, K. E. et al., J. Exp. Med., 187: 2009-2021(1998)). (NK cells are large granular lymphocytes, which lack a specificT cell receptor for antigen recognition, but possess cytolytic activityagainst cells such as tumor cells and virally infected cells.)Consistently, IP-10, Mig and I-TAC lack the ELR motif, an essentialbinding epitope in those CXC-chemokines that efficiently induceneutrophil chemotaxis (Clark-Lewis, I. et al., J. Biol. Chem. 266:23128-23134 (1991); Hebert, C. A. et al., J. Biol. Chem., 266:18989-18994 (1991); and Clark-Lewis, 1. et al., Proc. Natl. Acad. Sci.USA, 90: 3574-3577 (1993)). In addition, both recombinant human Mig andrecombinant human IP-10 have been reported to induce calcium flux intumor infiltrating lymphocytes (TIL) (Liao, F. et al., J. Exp. Med.,182: 1301-1314 (1995)). While IP-10 has been reported to inducechemotaxis of monocytes in vitro (Taub, D. D. et al., J. Exp. Med., 177:1809-1814 (1993), the receptor responsible has not been identified),human Mig and I-TAC appear highly selective, and do not show such aneffect (Liao, F. et al., J. Exp. Med., 182:1301-1314 (1995); Cole, K. E.et al., J. Exp. Med., 187: 2009-2021 (1998)). IP-10 expression isinduced in a variety of tissues in inflammatory conditions such aspsoriasis, fixed drug eruptions, cutaneous delayed-type hypersensitivityresponses and tuberculoid leprosy as well as tumors and in animal modelstudies, for example, experimental glomerulonephritis, and experimentalallergic encephalomyelitis. IP-10 has a potent in vivo antitumor effectthat is T cell dependent, is reported to be an inhibitor of angiogenesisin vivo and can induce chemotaxis and degranulation of NK cells invitro, suggesting a role as a mediator of NK cell recruitment anddegranulation (in tumor cell destruction, for example) (Luster, A. D.and P. Leder, J. Exp. Med., 178: 1057-1065 (1993); Luster, A. D. et al.,J. Exp. Med. 182: 219-231 (1995); Angiolillo, A. L. et al., J. Exp.Med., 182: 155-162 (1995); Taub, D. D. et al., J. Immunol., 155:3877-3888 (1995)). The expression patterns of IP-10, Mig and I-TAC arealso distinct from that of other CXC chemokines in that expression ofeach is induced by interferon-gamma (IFNδ), while the expression of IL-8is down-regulated by IFNδ (Luster, A. D. et al., Nature, 315: 672-676(1985); Farber, J. M., Proc. Natl. Acad. Sci. USA, 87: 5238-5242 (1990);Farber, J. M., Biochem. Biophys. Res. Commun., 192 (1): 223-230 (1993),Liao, F. et al., J. Exp. Med., 182: 1301-1314 (1995); Seitz, M. et al.,J. Clin. Invest., 87: 463-469 (1991); Galy, A. H. M. and H. Spits, J.Immunol., 147: 3823-3830 (1991); Cole, K. E. et al., J. Exp. Med., 187:2009-2021 (1998)).

Chemokines are recognized as the long-sought mediators for therecruitment of lymphocytes. Several CC-chemokines were found to elicitlymphocyte chemotaxis (Loetscher, P. et al., FASEB J., 8: 1055-1060(1994)), however, they are also active on granulocytes and monocytes(Uguccioni, M. et al., Eur. J. Immunol., 25: 64-68 (1995); Baggiolini,M. and C. A. Dahinden, Immunol. Today, 15: 127-133 (1994)). Thesituation is different for IP-10, Mig and I-TAC, which are selective intheir action on lymphocytes, including activated T lymphocytes and NKcells, and which bind CXCR3, a receptor which does not recognizenumerous other chemokines and which displays a selective pattern ofexpression.

In view of these observations, it is reasonable to conclude that theformation of the characteristic infiltrates in inflammatory lesions,such as, for example, delayed-type hypersensitivity lesions, sites ofviral infection and certain tumors is a process mediated via CXCR3 andregulated by CXCR3 expression. Lymphocytes, particularly T lymphocytes,bearing a CXCR3 receptor as a result of activation can be recruited intoinflammatory lesions, sites of infection and/or tumors by IP-10, Migand/or I-TAC, which can be induced locally by interferon-gamma. Thus,CXCR3 plays a role in the selective recruitment of lymphocytes,particularly effector cells such as activated or stimulated Tlymphocytes. Accordingly, activated and effector T cells have beenimplicated in a number of disease states such as graft-rejection,inflammation, rheumatoid arthritis, multiple sclerosis, inflammatorybowel disease (such as Crohn's disease and ulcerative colitis) andpsoriasis. Thus, CXCR3 represents a promising target for the developmentof novel therapeutics.

Reference is made to PCT Publication No. WO 93/10091 (Applicant: GlaxoGroup Limited, Published May 27, 1993) which discloses piperidine aceticacid derivatives as inhibitors of fibrinogen-dependent blood plateletaggregation having the formula:

An illustrative compound of that series is:

Reference is also made to PCT Publication No. WO 99/20606 (Applicant: J.Uriach & CIA. S. A., Published Apr. 29, 1999) which disclosespiperazines as platelet aggregation inhibitors having the formula:

Reference is also made to U.S. patent application No. US 2002/0018776 A1(Applicant: Hancock, et al. Published Feb. 14, 2002) which disclosesmethods of treating graft rejection.

Reference is also made to PCT Publication No. WO 03/098185 A2(Applicant: Renovar, Inc., Published Nov. 27, 2003) which disclosesmethods of diagnosing and predicting organ transplant rejection bydetection of chemokines, for example, CXCR3 and CCL chemokines in urine.

Reference is also made to PCT Publication No. WO 03/082335 A1(Applicant: Sumitomo Pharmaceuticals Co. Ltd., Published Oct. 9, 2003)which discloses methods of screening a CXCR3 ligand and methods ofdiagnosing type 2 diabetes by detecting the expression dose of a CXCR3ligand in a biological sample.

Reference is also made to PCT Publication No. WO 02/085861 (Applicant:Millennium Pharmaceuticals, Inc. Published Oct. 31, 2002) whichdiscloses imidazolidine compounds and their use as CXCR3 antagonistshaving the formula:

An illustrative compound of that series is:

Reference is also made to PCT Publication No. WO 03/101970 (Applicant:Smithkline Beecham Corporation, Published Dec. 11, 2003) which disclosesimidazolium compounds and their use as CXCR3 antagonists having theformula:

An illustrative example of that series is:

Reference is also made to U.S. patent application No. US 2003/0055054 A1(Applicant: Medina et al, Published Mar. 20, 2003) and related patentU.S. Pat. No. 6,794,379 B2 ((Applicant: Medina et al, Published Sep. 21,2004) which discloses compounds with CXCR3 activity having the formula:

An illustrative compound of that series is:

Reference is also made to U.S. Pat. No. 6,124,319 (Applicant: MacCoss etal., issued Sep. 6, 2000) which discloses compounds useful as chemokinereceptor modulators having the formula:

Reference is also made to PCT Publication WO 03/070242 A1 (Applicant:CELLTECH R & D limited, Published Aug. 28, 2003) which disclosescompounds useful as “chemokine receptor inhibitors for the treatment ofinflammatory diseases” having the formula:

Reference is also made to PCT Publication WO 04/074287 A1, WO 04/074273A1, WO 04/74278 (Applicant: AstraZeneca R & D Published Feb. 19^(th)2004) which discloses pyridine derivatives, processes for theirpreparation and use in the modulation of autoimmune disease, having theformula:

where R3 is phenyl, or a 5- or 6-membered aromatic ring with 1 or morenitrogen atoms.

There is a need for compounds that are capable of modulating CXCR3activity. For example, there is a need for new treatments and therapiesfor diseases and conditions associated with CXCR3 such as inflammatoryconditions (psoriasis and inflammatory bowel disease), autoimmunedisease (multiple sclerosis, rheumatoid arthritis) and graft rejection(allograft and zenograft rejections for example) as well as infectiousdiseases, cancers and tumors, fixed drug eruptions, cutaneousdelayed-type hypersensitivity responses, type I diabetes, viralmeningitis and tuberculoid leprosy.

There is a need for methods of treatment or prevention or ameliorationof one or more symptoms of diseases and conditions associated withCXCR3. There is a need for methods for modulating CXCR3 activity usingthe compounds provided herein.

SUMMARY OF THE INVENTION

In its many embodiments, the invention provides novel compounds of theFormula 1:

or a pharmaceutically acceptable salt, solvate or ester thereof,wherein:

Z is N, NO, NOH or C(R²⁹);

G represents a 5-membered heteroaryl or heterocyclenyl ring containingat least one —C═N— moiety as part of said heteroaryl or heterocyclenylring, said heteroaryl or heterocyclenyl ring optionally additionallycontaining on the ring (i.e., as ring moieties) one or more moietieswhich can be the same or different, each being independently selectedfrom the group consisting of N, N(→O), O, S, S(O) and S(O₂), furtherwherein said heteroaryl or heterocyclenyl ring can be either (i)unsubstituted, or (ii) optionally independently substituted on one ormore ring carbon atoms with one or more R⁹ substituents, or on one ormore ring nitrogen atoms with one or more R⁸ substituents, wherein saidR⁸ and R⁹ substituents can be the same or different;

R³, R⁴, R⁶ and R²⁹ moieties can be the same or different, each beingindependently selected from the group consisting of H, alkyl, alkylaryl,aralkyl, —CN, CF₃, haloalkyl, cycloalkyl, halogen, hydroxyalkyl,—N═CH—(R³¹), C(═O)N(R³⁰)₂, —N(R³⁰)₂, —OR³⁰, —SO₂(R³¹),—N(R³⁰)C(═O)N(R³⁰)₂ and —N(R³⁰)C(═O)R³¹;

the R⁸ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, alkenyl, alkylaryl,arylalkyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, —(CH₂)_(q)OH,—(CH₂)_(q)OR³¹, (CH₂)_(q)NH₂, —(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹,—(CH₂)_(q)C(═O)OR³¹, —(CH₂)_(q)SO₂R³¹, —(CH₂)_(q)NSO₂R³¹, or—(CH₂)_(q)SO₂NHR³¹;

the R⁹ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, alkenyl, alkylaryl,arylalkyl, alkoxy, amidinyl, aryl, cycloalkyl, cyano, heteroaryl,heterocyclyl, hydroxyl, —C(═O)N(R³⁰)₂, —C(═S)N(R³⁰)₂, —C(═O)alkyl,—(CH₂)_(q)OH, —(CH₂)_(q)OR³¹, (CH₂)_(q)NH₂, —(CH₂)_(q)NHR³¹,—(CH₂)_(q)C(═O)NHR³¹, (CH₂)_(q)SO₂R³¹, —(CH₂)_(q)NSO₂R³¹,—(CH₂)_(q)SO₂NHR³¹, —N(R³⁰)₂, —N(R³⁰)S(O₂)R³¹, —N(R³⁰)C(═O)N(R³⁰)₂,—OR³⁰—SO₂(R³¹), —SO₂N(R³⁰)₂, ═O and ═S;

the R¹⁰ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, cycloalkyl, aryl,heteroaryl, heterocyclenyl, heterocyclyl, alkylaryl, arylalkyl, —CO₂H,hydroxyalkyl, —C(═O)N(R³⁰)₂, —(CH₂)_(q)OH, —(CH₂)_(q)OR³¹—OR³⁰, halogen,═O, and —C(═O)R³¹;

the R¹¹ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, cycloalkyl, aryl,heteroaryl, heterocyclyl, heterocyclenyl, alkylaryl, arylalkyl,carboxamide, CO₂H, —(CH₂)_(q)OH, —(CH₂)_(q)OR³, —OR³⁰, halogen, ═O, and—C(═O)R³¹;

R¹² moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, —CN, —C(═O)N(R³⁰)₂,—(CH₂)_(q)OH, —(CH₂)_(q)OR³¹ and —S(O₂)R³¹;

ring D is a five to nine membered cycloalkyl, cycloalkenyl, aryl,heteroaryl, heterocyclenyl or heterocyclyl ring having 0-4 heteroatomsindependently selected from O, S or N, wherein ring D is unsubstitutedor optionally substituted with 1-5 independently selected R²⁰ moieties;

the R²⁰ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, alkenyl, alkylaryl,alkynyl, alkoxy, alkylamino, alkylthiocarboxy, alkylheteroaryl,alkylthio, alkylsulfinyl, alkylsulfonyl, alkoxycarbonyl, aminoalkyl,amidinyl, aralkyl, aralkenyl, aralkoxy, aralkoxycarbonyl, aralkylthio,aryl, aroyl, aryloxy, cyano, cycloalkyl, cycloalkenyl, formyl,guanidinyl, halogen, haloalkyl, heteroalkyl, heteroaryl, heterocyclyl,heterocyclenyl, hydroxyalkyl, hydroxamate, nitro, trifluoromethoxy,—(CH₂)_(q)OH, —(CH₂)_(q)OR³¹, —(CH₂)_(q)NH₂, —(CH₂)_(q)NHR³¹,—(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹, —(CH₂)_(q)NSO₂R³¹,—(CH₂)_(q)SO₂NHR³¹, -alkynyl C(R³¹)₂OR³¹, —C(═O)R³⁰—C(═O)N(R³⁰)₂,—C(═NR³⁰)NHR³⁰, —C(═NOH)N(R³⁰)₂, —C(═NOR³¹)N(R³⁰)₂, —C(═O)OR³⁰,—N(R³⁰)₂, —N(R³⁰)C(═O)R³¹, —NHC(═O)N(R³⁰), —N(R³⁰)C(═O)OR³¹,—N(R³⁰)C(═NCN)N(R³⁰)₂, —N(R³⁰)C(═O)N(R³⁰)SO₂(R³¹), —N(R³⁰)C(═O)N(R³⁰)₂,—N(R³⁰)SO₂(R³¹), —N(R³⁰)S(O)₂N(R³⁰)₂, —OR³⁰, —OC(═O)N(R³⁰)₂, —SR³⁰,—SO₂N(R³⁰)₂—SO₂(R³¹), —OSO₂(R³¹), and —OSi(R³⁰)₃; or alternatively twoR²⁰ moieties are linked together to form a five or six membered aryl,cycloalkyl, heterocyclyl, heterocyclenyl, or heteroaryl ring whereinsaid five or six membered aryl, cycloalkyl, heterocyclyl,heterocyclenyl, or heteroaryl ring is fused to ring D and the fused ringis optionally substituted with 0-4 R²¹ moieties;

the R²¹ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, alkenyl, alkylaryl,alkynyl, alkoxy, alkylamino, alkylthiocarboxy, alkylheteroaryl,alkylthio, alkylsulfinyl, alkylsulfonyl, alkoxycarbonyl, aminoalkyl,amidinyl, aralkyl, aralkenyl, aralkoxy, aralkoxycarbonyl, aralkylthio,aryl, aroyl, aryloxy, carboxamido, cyano, cycloalkyl, cycloalkenyl,formyl, guanidinyl, halogen, haloalkyl, heteroalkyl, heteroaryl,heterocyclyl, heterocyclenyl, hydroxyalkyl, hydroxamate, nitro,trifluoromethoxy, —(CH₂)_(q)OH, —(CH₂)_(q)OR³¹, —(CH₂)_(q)NH₂,—(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹,—(CH₂)_(q)NSO₂R³¹, —(CH₂)_(q)SO₂NHR³¹, -alkynylC(R³¹)₂OR³¹, —C(═O)R³⁰,—C(═O)N(R³⁰)₂, —C(═NR³⁰)NHR³⁰, —C(═NOH)N(R³)₂, —C(═NOR³¹)N(R³⁰)₂,—C(═O)OR³⁰—N(R³⁰)₂, —N(R³⁰)C(═O)R³¹, —NHC(═O)N(R³⁰)₂, —N(R³⁰)C(═O)OR³⁰,—N(R³⁰)C(═NCN)N(R³⁰)₂, —N(R³⁰)C(═O)N(R³⁰)SO₂(R³¹), —N(R³⁰)C(═O)N(R³⁰)₂,—N(R³⁰)SO₂(R³¹), —N(R³⁰)S(O)₂N(R³⁰)₂, —OR³⁰, —OC(═O)N(R³⁰)₂, —SR³⁰,—SO₂N(R³⁰)₂, —SO₂(R³¹), —OSO₂(R³¹), and —OSi(R³⁰)₃;

Y is selected from the group consisting of —(CR¹³R¹³)_(r)—,—CHR¹³C(═O)—, —(CHR¹³)_(r) O—, —(CHR¹³)_(r) N(R³⁰)—, —C(═O)—,—C(═NR³⁰)—, —C(═N—OR³⁰)—, —CH(C(═O)NHR³⁰)—, CH-heteroaryl-,—C(R¹³R¹³)_(r)C(R¹³)═C(R¹³)—, —(CHR¹³)_(r)C(═O)— and—(CHR¹³)_(r)N(H)C(═O)—; or alternatively Y is cycloalkyl,heterocyclenyl, or heterocyclyl wherein the cycloalkyl, heterocyclenyl,or heterocyclyl is fused with ring D;

the R¹³ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, alkylaryl, cycloalkyl,alkoxy, aryl, heteroaryl, heterocyclenyl, heterocyclyl, spiroalkyl, —CN,—CO₂H, —C(═O)R³⁰, —C(═O)N(R³⁰)₂, —(CHR³⁰)_(q)OH, —(CHR³⁰)_(q)OR³¹,—(CHR³⁰)_(q)NH₂, —(CHR³⁰)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹,—(CH₂)_(q)SO₂R³¹, —(CH₂)_(q)NSO₂R³, —(CH₂)_(q)SO₂NHR³¹, —NH₂, —N(R³⁰)₂,—N(R³⁰)C(═O)N(R³)₂, —N(R³⁰)SO₂(R³¹), —OH, OR³⁰, —SO₂N(R³¹)₂, and—SO₂(R³¹);

the R³⁰ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, alkylaryl, aryl,aralkyl, cycloalkyl, CN, —(CH₂)_(q)OH, —(CH₂)_(q)Oalkyl,—(CH₂)_(q)Oalkylaryl, —(CH₂)_(q)Oaryl, —(CH₂)_(q)Oaralkyl,—(CH₂)_(q)Ocycloalkyl, —(CH₂)_(q)NH₂, —(CH₂)_(q)NHalkyl,—(CH₂)_(q)N(alkyl)₂, —(CH₂)_(q)NHalkylaryl, —(CH₂)_(q)NHaryl,—(CH₂)_(q)NHaralkyl, —(CH₂)_(n)NHcycloalkyl, —(CH₂)_(q)C(═O)NHalkyl,—(CH₂)_(q)C(═O)N(alkyl)₂, —(CH₂)_(q)C(═O)NHalkylaryl,—(CH₂)_(q)C(—O)NHaryl, —(CH₂)_(q)C(═O)NHaralkyl,—(CH₂)_(q)C(═O)NHcycloalkyl, —(CH₂)_(q)SO₂alkyl, —(CH₂)_(q)SO₂alkylaryl,—(CH₂)_(q)SO₂aryl, —(CH₂)_(q)SO₂aralkyl, —(CH₂)_(q)SO₂cycloalkyl,—(CH₂)_(q)NSO₂alkyl, —(CH₂)_(q)NSO₂alkylaryl, —(CH₂)_(q)NSO₂aryl,—CH₂)_(q)NSO₂aralkyl, —(CH₂)_(q)NSO₂cycloalkyl, —(CH₂)_(q)SO₂NHalkyl,—(CH₂)_(q)SO₂NHalkylaryl, —(CH₂)_(q)SO₂NHaryl, —(CH₂)_(q)SO₂NHaralkyl,—(CH₂)_(q)SO₂NHcycloalkyl, heterocyclenyl, heterocyclyl, and heteroaryl;

the R³¹ moieties can be the same or different, each being independentlyselected from the group consisting of alkyl, alkylaryl, aryl, aralkyl,cycloalkyl, —(CH₂)_(q)OH, —(CH₂)_(q)Oalkyl, —(CH₂)_(q)Oalkylaryl,—(CH₂)_(q)Oaryl, —(CH₂)_(q)Oaralkyl, —(CH₂)_(q)Ocycloalkyl,—(CH₂)_(q)NH₂, —(CH₂)_(q)NHalkyl, —(CH₂)_(q)N(alkyl)₂,—(CH₂)_(q)NHalkylaryl, —(CH₂)_(q)NHaryl, —(CH₂)_(q)NHaralkyl,—(CH₂)_(q)NHcycloalkyl, —(CH₂)_(q)C(═O)NHalkyl,—(CH₂)_(q)C(═O)N(alkyl)₂, —(CH₂)_(q)C(═O)NHalkylaryl,—(CH₂)_(q)C(═O)NHaryl, —(CH₂)_(n)C(═O)NHaralkyl,—(CH₂)_(q)C(═O)NHcycloalkyl, —(CH₂)_(q)SO₂alkyl, —(CH₂)_(q)SO₂alkylaryl,—(CH₂)_(q)SO₂aryl, —(CH₂)_(q)SO₂aralkyl, —(CH₂)_(q)SO₂cycloalkyl,—(CH₂)_(q)NSO₂alkyl, —(CH₂)_(q)NSO₂alkylaryl, —(CH₂)_(q)NSO₂aryl,—(CH₂)_(q)NSO₂aralkyl, —(CH₂)_(q)NSO₂cycloalkyl, —(CH₂)_(q)SO₂NHalkyl,—(CH₂)_(q)SO₂NHalkylaryl, —(CH₂)_(q)SO₂NHaryl, —(CH₂)_(q)SO₂NHaralkyl,—(CH₂)_(q)SO₂NHcycloalkyl, heterocyclenyl, heterocyclyl, and hetroaryl;

m is 0 to 4;

n is 0 to 4;

each q can be the same or different, each being independently selectedfrom 1 to 5; and

r is 1 to 4;

with the proviso that there are no two adjacent double bonds in anyring, and that when a nitrogen is substituted by two alkyl groups, saidtwo alkyl groups may be optionally joined to each other to form a ring.

The term “G represents a 5-membered heteroaryl or heterocyclenyl ringcontaining at least one —C═N— moiety” means that G represents, in anon-limiting manner, moieties such as dihydroimidizole, imidazole,dihydrooxazole, oxazole, dihydrooxadiazole, oxadiazole, dihydrothiazole,thiazole, triazole, tetrazole and the like. These moieties may beoptionally substituted on the ring carbon(s) with one or more R⁹ groupsas stated above, or on the ring nitrogen(s) with one or more R⁸ groupsas stated above.

The term “said heteroaryl or heterocyclenyl ring optionally additionallycontaining on the ring (i.e., as ring moieties) one or more moietieswhich can be the same or different, each being independently selectedfrom the group consisting of N, N(→O), O, S, S(O) and S(O₂)” means thatthe N, N(→O), O, S, S(O) and S(O₂) are present as ring ‘atoms’ and notas substituents.

A further feature of the invention is a pharmaceutical compositioncontaining as active ingredient at least one compound of Formula 1together with at least one pharmaceutically acceptable carrier orexcipient.

The invention provides methods of preparing compounds of Formula 1, aswell as methods for treating diseases, for example, treatment (e.g.,palliative therapy, curative therapy, prophylactic therapy) of certaindiseases and conditions e.g., inflammatory diseases (e.g., psoriasis,inflammatory bowel disease), autoimmune diseases (e.g., rheumatoidarthritis, multiple sclerosis), graft rejection (e.g., allograftrejection, xenograft rejection), ophthalmic inflammation or dry eye,infectious diseases and tumors. The invention provides a method oftreating a CXCR3 chemokine mediated disease in a patient in need of suchtreatment comprising administering to the patient a therapeuticallyeffective amount of at least one compound of Formula 1, or apharmaceutically acceptable salt, solvate or ester thereof.

The invention provides methods of treating diseases, for example,treatment (e.g., palliative therapy, curative therapy, prophylactictherapy) of certain diseases and conditions such as inflammatorydiseases (e.g., psoriasis, inflammatory bowel disease), autoimmunediseases (e.g., rheumatoid arthritis, multiple sclerosis), graftrejection (e.g., allograft rejection, xenograft rejection), infectiousdiseases as well as cancers and tumors, fixed drug eruptions, cutaneousdelayed-type hypersensitivity responses, ophthalmic inflammation or dryeye, type I diabetes, viral meningitis and tuberculoid leprosycomprising administering: (a) a therapeutically effective amount of atleast one compound according to Formula 1, or a pharmaceuticallyacceptable salt, solvate or ester thereof concurrently or sequentiallywith (b) at least one medicament selected from the group consisting of:disease modifying antirheumatic drugs; nonsteroidal anti-inflammatorydrugs; COX-2 selective inhibitors; COX-1 inhibitors; immunosuppressives(such as cyclosporins and methotrexate); steroids (includingcorticosteroids such as glucorticoids); PDE IV inhibitors, anti-TNF-αcompounds, TNF-α-convertase (TACE) inhibitors, MMP inhibitors, cytokineinhibitors, glucocorticoids, other chemokine inhibitors such as CCR2 andCCR5, CB2-selective inhibitors, p38 inhibitors, biological responsemodifiers; anti-inflammatory agents and therapeutics.

The invention also provides a method of modulating (inhibiting orpromoting) an inflammatory response in an individual in need of suchtherapy. The method comprises administering a therapeutically effectiveamount of a compound (e.g., small organic molecule) which inhibits orpromotes mammalian CXCR3 function in an individual in need thereof. Alsodisclosed is a method of inhibiting or blocking T-cell mediatedchemotaxis in a patient in need of such treatment comprisingadministering to the patient a therapeutically effective amount of acompound of Formula 1 or a pharmaceutically acceptable salt, solvate orester thereof.

Also disclosed is a method of treating inflammatory bowel disease (suchCrohn's disease, ulcerative colitis) in a patient in need of suchtreatment comprising administering to the patient a therapeuticallyeffective amount of at least one compound of Formula 1, or apharmaceutically acceptable salt, solvate or ester thereof.

Also disclosed is a method of treating inflammatory bowel disease in apatient in need of such treatment comprising administering to thepatient a therapeutically effective amount of: (a) at least one compoundof Formula 1, or a pharmaceutically acceptable salt, solvate or esterthereof concurrently or sequentially with (b) at least one compoundselected from the group consisting of: sulfasalazine, 5-aminosalicylicacid, sulfapyridine, anti-TNF compounds, anti-IL-12 compounds,corticosteroids, glucocorticoids, T-cell receptor directed therapies(such as anti-CD3 antibodies), immunosuppressives, methotrexate,azathioprine, and 6-mercaptopurines.

Also disclosed is a method of treating graft rejection in a patient inneed of such treatment comprising administering to the patient atherapeutically effective amount of at least one compound of Formula 1,or a pharmaceutically acceptable salt, solvate or ester thereof.

Also disclosed is a method of treating graft rejection in a patient inneed of such treatment comprising administering to the patient atherapeutically effective amount of: (a) at least one compound ofFormula 1, or a pharmaceutically acceptable salt, solvate or esterthereof concurrently or sequentially with (b) at least one compoundselected from the group consisting of: cyclosporine A, FK-506, FTY720,beta-interferon, rapamycin, mycophenolate, prednisolone, azathioprine,cyclophosphamide and an antilymphocyte globulin.

Also disclosed is a method of treating multiple sclerosis in a patientin need of such treatment the method comprising administering to thepatient a therapeutically effective amount of: (a) a therapeuticallyeffective amount of at least one compound of Formula 1, or apharmaceutically acceptable salt, solvate or ester thereof concurrentlyor sequentially with (b) at least one compound selected from the groupconsisting of: beta-interferon, glatiramer acetate, corticosteroids,glucocorticoids, methotrexate, azothioprine, mitoxantrone, VLA-4inhibitors, FTY720, anti-IL-12 inhibitors, and CB2-selective inhibitors.

Also disclosed is a method of treating multiple sclerosis in a patientin need of such treatment the method comprising administering to thepatient a therapeutically effective amount of: (a) a therapeuticallyeffective amount of at least one compound of Formula 1, or apharmaceutically acceptable salt, solvate or ester thereof concurrentlyor sequentially with (b) at least one compound selected from the groupconsisting of: methotrexate, cyclosporin, leflunomide, sulfasalazine,corticosteroids, β-methasone, β-interferon, glatiramer acetate,prednisone, etonercept, and infliximab.

Also disclosed is a method of treating rheumatoid arthritis in a patientin need of such treatment the method comprising administering to thepatient a therapeutically effective amount of: (a) at least one compoundof Formula 1, or a pharmaceutically acceptable salt, solvate or esterthereof concurrently or sequentially with (b) at least one compoundselected from the group consisting of: non-steroidal anti-inflammatoryagents, COX-2 inhibitors, COX-1 inhibitors, immunosuppressives,cyclosporine, methotrexate, steroids, PDE IV inhibitors, anti-TNF-αcompounds, MMP inhibitors, corticosteroids, glucocorticoids, chemokineinhibitors, CB2-selective inhibitors, caspase (ICE) inhibitors and otherclasses of compounds indicated for the treatment of rheumatoidarthritis.

Also disclosed is a method of treating psoriasis in a patient in need ofsuch treatment the method comprising administering to the patient atherapeutically effective amount of: a) at least one compound of Formula1, or a pharmaceutically acceptable salt, solvate or ester thereofconcurrently or sequentially with (b) at least one compound selectedfrom the group consisting of: immunosuppressives, cyclosporins,methotrexate, steroids, corticosteroids, anti-TNF-α compounds, anti-ILcompounds, anti-IL-23 compounds, vitamin A and D compounds andfumarates.

Also disclosed is a method of treating ophthalmic inflammation(including, for e.g., uveitis, posterior segment intraocularinflammation, Sjogren's syndrome) or dry eye in a patient in need ofsuch treatment the method comprising administering to the patient atherapeutically effective amount of: a) at least one compound accordingto Formula 1, or a pharmaceutically acceptable salt, solvate or esterthereof concurrently or sequentially with (b) at least one compoundselected from the group consisting of: immunosuppressives, cyclosporins,methotrexate, FK506, steroids, corticosteroids, and anti-TNF-αcompounds.

Also disclosed is a method of treating a disease selected from the groupconsisting of: inflammatory disease, rheumatoid arthritis, multiplesclerosis, inflammatory bowel disease, graft rejection, psoriasis, fixeddrug eruptions, cutaneous delayed-type hypersensitivity responses,ophthalmic inflammation (including e.g., uveitis, posterior segmentintraocular inflammation, and Sjogren's syndrome), tuberculoid leprosyand cancer in a patient in need of such treatment, such methodcomprising administering to the patient an effective amount of at leastone compound according to Formula 1, or a pharmaceutically acceptablesalt, solvate or ester thereof.

The invention also provides a method of treating a disease selected fromthe group consisting of: inflammatory disease, rheumatoid arthritis,multiple sclerosis, inflammatory bowel disease, graft rejection,psoriasis, fixed drug eruptions, cutaneous delayed-type hypersensitivityresponses and tuberculoid leprosy, ophthalmic inflammation, type Idiabetes, viral meningitis and cancer in a patient in need of suchtreatment, such method comprising administering to the patient aneffective amount of (a) at least one compound according to Formula 1, ora pharmaceutically acceptable salt, solvate or ester thereofconcurrently or sequentially with (b) at least one medicament selectedfrom the group consisting of: disease modifying antirheumatic drugs;nonsteroidal antiinflammatory drugs; COX-2 selective inhibitors; COX-1inhibitors; immunosuppressives; steroids; PDE IV inhibitors, anti-TNF-αcompounds, MMP inhibitors, corticosteroids, glucocorticoids, chemokineinhibitors, CB2-selective inhibitors, biological response modifiers;anti-inflammatory agents and therapeutics.

DETAILED DESCRIPTION OF THE INVENTION

The terms used herein have their ordinary meaning and the meaning ofsuch terms is independent at each occurrence thereof. Thatnotwithstanding and except where stated otherwise, the followingdefinitions apply throughout the specification and claims. Chemicalnames, common names, and chemical structures may be used interchangeablyto describe the same structure. These definitions apply regardless ofwhether a term is used by itself or in combination with other terms,unless otherwise indicated. Hence, the definition of “alkyl” applies to“alkyl” as well as the “alkyl” portions of “hydroxyalkyl,” “haloalkyl,”“alkoxy,” etc.

As used above, and throughout the specification, the following terms,unless otherwise indicated, shall be understood to have the followingmeanings:

“Acyl” means an H—C(═O)—, alkyl-C(═O)—, alkenyl-C(═O)—, alkynyl-C(═O)—,cycloalkyl-C(═O)—, cycloalkenyl-C(═O)—, or cycloalkynyl-C(═O)— group inwhich the various groups are as previously described. The bond to theparent moiety is through the carbonyl carbon atom. Preferred acylscontain a lower alkyl. Non-limiting examples of suitable acyl groupsinclude formyl, acetyl, propanoyl, 2-methylpropanoyl, butanoyl andcyclohexanoyl.

“Alkenyl” means an aliphatic hydrocarbon group containing at least onecarbon-carbon double bond and which may be straight or branched andcomprising about 2 to about 15 carbon atoms in the chain. Preferredalkenyl groups have about 2 to about 12 carbon atoms in the chain; andmore preferably about 2 to about 6 carbon atoms in the chain. Branchedmeans that one or more lower alkyl groups such as methyl, ethyl orpropyl, are attached to a linear alkenyl chain. “Lower alkenyl” meansabout 2 to about 6 carbon atoms in the chain which may be straight orbranched. The alkenyl group may be substituted by one or moresubstituents which may be the same or different, each substituent beingindependently selected from the group consisting of alkyl, alkenyl,alkynyl, alkoxyl, aryl, aryloxy, cycloalkyl, cycloalkenyl, cyano,heteroaryl, heterocyclyl, amino, aminosulfonyl, halo, carboxyl,carboxyalkyl (non-limiting example(s) include ester), alkoxycarbonyl,hydroxyalkyl, carbonyl (non-limiting example(s) include ketone),—C(═O)heterocyclyl, formyl (non-limiting example(s) include aldehyde),carboxamido (i.e amido, —C(═O)NH₂), —C(═O)N(alkyl)₂, —C(═O)NH(alkyl),—C(═O)N(cycloalkyl)₂, —C(═O)NH(cycloalkyl), —NHC(═O)alkyl, urea (e.g—NH(C═O)NH₂, —NH(C═O)NH(alkyl), —NH(C═O)NH(alkyl)₂,—NH(C═O)NH(heteroaryl), —NH(C═O)NH(heterocyclyl)), guanidinyl,—NHC(═NCN)NH₂, —NHC(═NCN)N(alkyl)₂, carbamoyl (i.e —CO₂NH₂),NHC(═O)Oalkyl, —CO₂N(alkyl)₂, —NHC(═O))NH—S(O)₂alkyl,—NHC(═O)N(alkyl)₂-S(O)₂alkyl, —NH—S(O)₂alkyl, —NH—S(O)₂heteroaryl,—N(alkyl)-S(O)₂alkyl, —NH—S(O)₂aryl, —N(alkyl)-S(O)₂aryl, —NH—S(O)₂NH₂,—NH—S(O)₂NHalkyl, —NH—S(O)₂N(alkyl)₂, alkylthiocarboxy, —S(O)₂alkyl,—S(O)₂aryl, —OS(O)₂alkyl, —OS(O)₂aryl, sulfonyl urea (non-limitingexample(s) include NHC(═S)NHalkyl). Non-limiting examples of suitablealkenyl groups include ethenyl, propenyl, n-butenyl, 3-methylbut-2-enyl,n-pentenyl, octenyl and decenyl.

“Alkyl” means an aliphatic hydrocarbon group which may be straight orbranched or a combination thereof, and comprising about 1 to about 20carbon atoms in the chain. Preferred alkyl groups contain about 1 toabout 12 carbon atoms in the chain. More preferred alkyl groups containabout 1 to about 6 carbon atoms in the chain. Branched means that one ormore lower alkyl groups such as methyl, ethyl or propyl, are attached toa linear alkyl chain. “Lower alkyl” means a group having about 1 toabout 6 carbon atoms in the chain which may be straight or branched. Thealkyl group may be substituted by one or more substituents which may bethe same or different each substituent being independently selected fromthe group consisting of alkyl, alkenyl, alkynyl, alkoxyl, aryl, aryloxy,cycloalkyl, cycloalkenyl, cyano, heteroaryl, heterocyclyl, amino,—NH(alkyl), —N(alkyl)₂, —NH(cycloalkyl), —N(cycloalkyl)₂, —NH(aryl),—N(aryl)₂, —NH(heteroaryl), —N(heteroaryl)₂, —NH(heterocyclyl),N(heterocyclyl)₂, halo, hydroxy, carboxyl, carboxyalkyl (non-limitingexample(s) include ester), alkoxycarbonyl, hydroxyalkyl, carbonyl(non-limiting example(s) include ketone), —C(═O)heterocyclyl, formyl,carboxamido (i.e amido, —C(═O)NH₂, —C(═O)N(alkyl)₂, —C(═O)NH(alkyl),—C(═O)N(cycloalkyl)₂, —C(═O)NH(cycloalkyl)), —NHC(═O)alkyl, amidinyl,hydrazinyl, hydroxamate, —NHC(═O)H, —NHC(═O)alkyl, urea (e.g—NH(C═O)NH₂, —NH(C═O)NH(alkyl), —NH(C═O)NH(alkyl)₂,—NH(C═O)NH(heteroaryl), —NH(C═O)NH(heterocyclyl)), guanidinyl,—NHC(═NCN)NH₂, —NHC(═NCN)N(alkyl)₂, carbamoyl (i.e —CO₂NH₂),—NHC(═O)Oalkyl, —CO₂N(alkyl)₂, —NHC(═O)NH—S(O)₂alkyl,—NHC(═O)N(alkyl)-S(O)₂alkyl, —NH—S(O)₂alkyl, —NH—S(O)₂heteroaryl,—N(alkyl)-S(O)₂alkyl, —NH—S(O)₂aryl, —N(alkyl)-S(O)₂aryl, —NH—S(O)₂NH₂,—NH—S(O)₂NHalkyl, —NH—S(O)₂N(alkyl)₂, thio, alkylthio, alkylthiocarboxy,—S(O)alkyl, —S(O)₂alkyl, —S(O)₂aryl, —OS(O)₂alkyl, —OS(O)₂aryl, sulfonylurea (non-limiting example(s) include —NHC(═S)NHalkyl) and OSi(alkyl)₃.Non-limiting examples of suitable alkyl groups include methyl, ethyl,n-propyl, isopropyl, n-butyl, t-butyl, n-pentyl, heptyl, nonyl, decyl,fluoromethyl, trifluoromethyl and cyclopropylmethyl.

“Alkylheteroaryl” means an alkyl-heteroaryl-group wherein the alkyl isas previously described and the bond to the parent moiety is through theheteroaryl group.

“Alkylamino” means an —NH₂ or —NH₃+ group in which one or more of thehydrogen atoms on the nitrogen is replaced by an alkyl group as definedabove. The bond to the parent is through the nitrogen.

“Alkylaryl” means an alkyl-aryl-group in which the alkyl and aryl are asdescribed herein. Preferred alkylaryls comprise a lower alkyl group.Non-limiting examples of suitable alkylaryl groups include o-tolyl,p-tolyl and xylyl. The bond to the parent moiety is through the aryl.

“Alkylthio” means an alkyl-S— group in which the alkyl group is asdescribed herein. Non-limiting examples of suitable alkylthio groupsinclude methylthio, ethylthio, i-propylthio and heptylthio. The bond tothe parent moiety is through the sulfur.

“Alkylthiocarboxy” means an alkyl-S—C(═O)O— group. Preferred groups arethose in which the alkyl group is lower alkyl. The bond to the parentmoiety is through the carboxy.

“Alkylsulfonyl” means an alkyl-S(O)₂— group. Preferred groups are thosein which the alkyl group is lower alkyl. The bond to the parent moietyis through the sulfonyl.

“Alkylsulfinyl” means an alkyl-S(O)— group. Preferred groups are thosein which the alkyl group is lower alkyl. The bond to the parent moietyis through the sulfinyl.

“Alkynyl” means an aliphatic hydrocarbon group containing at least onecarbon-carbon triple bond and which may be straight or branched andcomprising about 2 to about 15 carbon atoms in the chain. Preferredalkynyl groups have about 2 to about 12 carbon atoms in the chain; andmore preferably about 2 to about 4 carbon atoms in the chain. Branchedmeans that one or more lower alkyl groups such as methyl, ethyl orpropyl, are attached to a linear alkynyl chain. “Lower alkynyl” meansabout 2 to about 6 carbon atoms in the chain which may be straight orbranched. Non-limiting examples of suitable alkynyl groups includeethynyl, propynyl, 2-butynyl, 3-methylbutynyl, n-pentynyl, and decynyl.The alkynyl group may be substituted by one or more substituents whichmay be the same or different, each substituent being independentlyselected from the group consisting of alkyl, alkoxyl, aryl, aryloxy,cycloalkyl, cycloalkenyl, cyano, heteroaryl, heterocyclyl, —NH(alkyl),—N(alkyl)₂, —NH(cycloalkyl), —N(cycloalkyl)₂, —NH(aryl), —N(aryl)₂,—NH(heteroaryl), —N(heteroaryl)₂, —NH(heterocyclyl), N(heterocyclyl)₂,alkoxycarbonyl, hydroxyalkyl, carbonyl (non-limiting example(s) includeketone), —C(═O)heterocyclyl, carboxamido (i.e amido, —C(═O)NH₂),—C(═O)N(alkyl)₂, —C(═O)NH(alkyl),—C(═O)N(cycloalkyl)₂-C(═O)NH(cycloalkyl), alkylC(═O)NH—, —NHC(═O)alkyl,urea (e.g —NH(C═O)NH₂) —NH(C═O)NH(alkyl), —NH(C═O)NH(alkyl)₂,—NH(C═O)NH(heteroaryl), —NH(C═O)NH(heterocyclyl), —S(O)₂alkyl, and—S(O)₂aryl-.

“Alkoxy” means an alkyl-O— group in which the alkyl group is aspreviously described. Non-limiting examples of suitable alkoxy groupsinclude methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, heptoxy andmethylhydroxy. The bond to the parent moiety is through the etheroxygen.

“Alkoxycarbonyl” means an alkyl-O—C(═O)— group. Non-limiting examples ofsuitable alkoxycarbonyl groups include methoxycarbonyl andethoxycarbonyl. The bond to the parent moiety is through the carbonyl.

“Aminoalkyl” means an amine-alkyl-group in which alkyl is as previouslydefined. Preferred aminoalkyls contain lower alkyl. Non-limitingexamples of suitable aminoalkyl groups include aminomethyl and2-Dimethlylamino-2-ethyl. The bond to the parent moiety is through thealkyl.

“Amidinyl” means —C(═NR)NHR group. The R groups are defined as H, alkyl,alkylaryl, heteroaryl, hydroxyl, alkoxy, amino, ester, —NHSO₂alkyl,—NHSO₂Aryl, —NHC(═O)NHalkyl, and —NHalkyl. The bond to the parent moietyis through the carbon.

“Aralkyl” or “arylalkyl” means an aryl-alkyl-group in which the aryl andalkyl are as previously described. Preferred aralkyls comprise a loweralkyl group attached to the aryl group. Non-limiting examples ofsuitable aralkyl groups include benzyl, 2-phenethyl andnaphthalenylmethyl. The bond to the parent moiety is through the alkyl.

“Aralkenyl” means an aryl-alkenyl-group in which the aryl and alkenylare as previously described. Preferred aralkenyls contain a loweralkenyl group. Non-limiting examples of suitable aralkenyl groupsinclude 2-phenethenyl and 2-naphthylethenyl. The bond to the parentmoiety is through the alkenyl.

“Aralkylthio” means an aralkyl-S— group in which the aralkyl group is aspreviously described. Non-limiting example of a suitable aralkylthiogroup is benzylthio. The bond to the parent moiety is through thesulfur.

“Aralkoxy” means an aralkyl-O— group in which the aralkyl group is asdescribed above. The bond to the parent moiety is through the oxygengroup.

“Aralkoxycarbonyl” means an aralkyl-O—C(═O)— group. Non-limiting exampleof a suitable aralkoxycarbonyl group is benzyloxycarbonyl. The bond tothe parent moiety is through the carbonyl.

“Aroyl” means an aryl-C(═O)— group in which the aryl group is aspreviously described. The bond to the parent moiety is through thecarbonyl. Non-limiting examples of suitable groups include benzoyl and1- and 2-naphthoyl.

“Aryl” (sometimes abbreviated “Ar”) means an aromatic monocyclic ormulticyclic ring system comprising about 6 to about 14 carbon atoms,preferably about 6 to about 10 carbon atoms. The aryl group can beoptionally substituted with one or more “ring system substituents” whichmay be the same or different, and are as defined herein. Non-limitingexamples of suitable aryl groups include phenyl and naphthyl.

“Aryloxy” means an aryl-O— group in which the aryl group is aspreviously described. Non-limiting examples of suitable aryloxy groupsinclude phenoxy and naphthoxy. The bond to the parent moiety is throughthe ether oxygen.

“Arylsulfonyl” means an aryl-S(O)₂— group. The bond to the parent moietyis through the sulfonyl.

“Arylsulfinyl” means an aryl-S(O)— group. The bond to the parent moietyis through the sulfinyl.

“Arylthio” means an aryl-S— group in which the aryl group is aspreviously described. Non-limiting examples of suitable arylthio groupsinclude phenylthio and naphthylthio. The bond to the parent moiety isthrough the sulfur.

“Carboxyalkyl” means an alkyl-C(═O)O— group. The bond to the parentmoiety is through the carboxy.

Carbamates and urea substituents refer to groups with oxygens andnitrogens respectively adjacent an amide; representative carbamate andurea substituents include the following:

“Cycloalkyl” means a non-aromatic mono- or multicyclic ring systemcomprising about 3 to about 10 carbon atoms, preferably about 5 to about10 carbon atoms. Preferred cycloalkyl rings contain about 5 to about 7ring atoms. The cycloalkyl can be optionally substituted with one ormore “ring system substituents” which may be the same or different, andare as defined above. Non-limiting examples of suitable monocycliccycloalkyls include cyclopropyl, cyclopentyl, cyclohexyl, cycloheptyland the like. Non-limiting examples of suitable multicyclic cycloalkylsinclude 1 decalin, norbornyl, adamantyl and the like.

“Cycloalkenyl” means a non-aromatic mono or multicyclic ring systemcomprising about 3 to about 10 carbon atoms, preferably about 5 to about10 carbon atoms which contains at least one carbon-carbon double bond.Preferred cycloalkenyl rings contain about 5 to about 7 ring atoms. Thecycloalkenyl can be optionally substituted with one or more “ring systemsubstituents” which may be the same or different, and are as definedabove. Non-limiting examples of suitable monocyclic cycloalkenylsinclude cyclopentenyl, cyclohexenyl, cycloheptenyl, and the like.Non-limiting example of a suitable multicyclic cycloalkenyl isnorbornylenyl. The term “cycloalkenyl” additionally means moieties suchas cyclobutenedione, cyclopentenone, cyclopentenedione and the like.

“Halogen” (or halo) means fluorine, chlorine, bromine, or iodine.Preferred are fluorine, chlorine and bromine.

“Haloalkyl” means an alkyl as defined above wherein one or more hydrogenatoms on the alkyl is replaced by a halo group defined above.Non-limiting examples include trifluoromethyl, 2,2,2-trifluoroethyl,2-chloropropyl and alike.

“Heteroaryl” means an aromatic monocyclic or multicyclic ring systemcomprising about 5 to about 14 ring atoms, preferably about 5 to about10 ring atoms, in which one or more of the ring atoms is an elementother than carbon, for example nitrogen, oxygen or sulfur, alone or incombination. Preferred heteroaryls contain about 5 to about 6 ringatoms. The “heteroaryl” can be optionally substituted by one or more“ring system substituents” which may be the same or different, and areas defined herein. The prefix aza, oxa or thia before the heteroarylroot name means that at least a nitrogen, oxygen or sulfur atomrespectively, is present as a ring atom. The nitrogen or sulfur atom ofthe heteroaryl can be optionally oxidized to the corresponding N-oxide,S-oxide or S,S-dioxide. Non-limiting examples of suitable heteroarylsinclude pyridyl, pyrazinyl, furanyl, thienyl, pyrimidinyl, isoxazolyl,isothiazolyl, oxazolyl, thiazolyl, pyrazolyl, furazanyl, pyrrolyl,pyrazolyl, triazolyl, 1,2,4-thiadiazolyl, pyridazinyl, quinoxalinyl,phthalazinyl, imidazo[1,2-a]pyridinyl, imidazo[2,1-b]thiazolyl,benzofurazanyl, indolyl, azaindolyl, benzimidazolyl, benzothienyl,quinolinyl, imidazolyl, thienopyridyl, quinazolinyl, thienopyrimidyl,pyrrolopyridyl, imidazopyridyl, isoquinolinyl, benzoazaindolyl,1,2,4-triazinyl, benzothiazolyl and the like.

“Heterocyclenyl” means a partially unsaturated monocyclic or partiallyunsaturated multicyclic ring system comprising about 5 to about 14 ringatoms, preferably about 5 to about 10 ring atoms, in which one or moreof the ring atoms is an element other than carbon, for example nitrogen,oxygen or sulfur, alone or in combination. Preferred heterocyclenylscontain about 5 to about 6 ring atoms and 1-3 double bonds. Preferredheterocyclenyls also contain at least one —C═N as part of the ring. The“heterocyclenyl” can be optionally substituted by one or more “ringsystem substituents” which may be the same or different, and are asdefined herein. The prefix aza, oxa or thia before the heterocyclenylroot name means that at least a nitrogen, oxygen or sulfur atomrespectively, is present as a ring atom. The nitrogen or sulfur atom ofthe heteroaryl can be optionally oxidized to the corresponding N-oxide,S-oxide or S,S-dioxide. Non-limiting examples of suitableheterocyclenyls include dihydroimidizole, dihydrooxazole,dihydrooxadiazole, dihydrothiazole, and the like.

“Heterocyclyl” (or heterocycloalkyl) means a non-aromatic saturatedmonocyclic or multicyclic ring system comprising about 3 to about 10ring atoms, preferably about 5 to about 10 ring atoms, in which one ormore of the atoms in the ring system is an element other than carbon,for example nitrogen, oxygen or sulfur, alone or in combination.Preferred heterocyclyls contain about 5 to about 6 ring atoms. Theprefix aza, oxa or thia before the heterocyclyl root name means that atleast a nitrogen, oxygen or sulfur atom respectively is present as aring atom. The heterocyclyl can be optionally substituted by one or more“ring system substituents” which may be the same or different, and areas defined herein. The nitrogen or sulfur atom of the heterocyclyl canbe optionally oxidized to the corresponding N-oxide, S-oxide orS,S-dioxide. Non-limiting examples of suitable monocyclic heterocyclylrings include piperidyl, pyrrolidinyl, piperazinyl, morpholinyl,oxazolidinyl, imidazolidinyl, thiomorpholinyl, thiazolidinyl,1,3-dioxolanyl, 1,4-dioxanyl, tetrahydrofuranyl, tetrahydrothiophenyl,tetrahydrothiopyranyl, and the like. Also included are ring systemscomprising about 3 to about 10 ring atoms, preferably about 5 to about10 ring atoms, in which one or more of the atoms in the ring system isan element other than carbon, for example nitrogen, oxygen or sulfuratom, alone or in combination, and which contains at least onecarbon-carbon double bond or carbon-nitrogen double bond. There are noadjacent oxygen and/or sulfur atoms present in the ring system.Non-limiting examples of suitable monocyclic azaheterocyclic (i.e.,azaheterocyclyl) groups include 1,2,3,4-tetrahydropyridine,1,2-dihydropyridyl, 1,4-dihydropyridyl, 1,2,3,6-tetrahydropyridine,1,4,5,6-tetrahydropyrimidine, dihydro-2-pyrrolinyl,dihydro-3-pyrrolinyl, dihydro-2-imidazolinyl, dihydro-2-pyrazolinyl,dihydro-4,5-triazolyl and the like. Non-limiting examples of suitableoxaheterocyclic (i.e., oxaheterocyclyl) groups include3,4-dihydro-2H-pyran, dihydrofuranyl, fluorodihydrofuranyl, and thelike. Non-limiting example of a suitable multicyclic oxaheterocyclicgroup is 7-oxabicyclo[2.2.1]heptenyl. Non-limiting examples of suitablemonocyclic thiaheterocyclic (i.e., thiaheterocyclyl) rings includedihydrothiophenyl, dihydrothiopyranyl, and the like.

“Heteroaralkyl” means a heteroaryl-alkyl-group in which the heteroaryland alkyl are as previously described. Preferred heteroaralkyls containa lower alkyl group. Non-limiting examples of suitable aralkyl groupsinclude pyridylmethyl, 2-(furan-3-yl)ethyl and quinolin-(3-yl)methyl.The bond to the parent moiety is through the alkyl.

“Heteroaralkenyl” means an heteroaryl-alkenyl-group in which theheteroaryl and alkenyl are as previously described. Preferredheteroaralkenyls contain a lower alkenyl group. Non-limiting examples ofsuitable heteroaralkenyl groups include 2-(pyrid-3-yl)ethenyl and2-(quinolin-3-yl)ethenyl. The bond to the parent moiety is through thealkenyl.

“Hydroxyalkyl” means a HO-alkyl-group in which alkyl is as previouslydefined. Preferred hydroxyalkyls contain lower alkyl. Non-limitingexamples of suitable hydroxyalkyl groups include hydroxymethyl and2-hydroxyethyl. The bond to the parent moiety is through the alkyl.

“Hydroxamate” means an alkyl-C(═O)NH—O— group. The bond to the parentmoiety is through the oxygen group.

“Ring system substituent” means a substituent attached to an aromatic ornon-aromatic ring system which, for example, replaces an availablehydrogen on the ring system. Ring system substituents may be the same ordifferent, each being independently selected from the group consistingof H, alkyl, alkenyl, alkynyl, alkoxyl, aryl, aroyl, aryloxy,cycloalkyl, cycloalkenyl, heteroaryl, heterocyclyl, alkylaryl,alkylheteroaryl, aralkyl, aralkenyl, aralkoxy, aralkoxycarbonyl, amino,—NH(alkyl), —N(alkyl)₂, —NH(cycloalkyl), —N(cycloalkyl)₂, —NH(aryl),—N(aryl)₂, —NH(heteroaryl), —N(heteroaryl)₂, —NH(heterocyclyl),N(heterocyclyl)₂, halo, hydroxy, carboxyl, carboxyalkyl (non-limitingexample(s) include ester), cyano, alkoxycarbonyl, hydroxyalkyl, carbonyl(non-limiting example(s) include ketone), —C(═O)heterocyclyl, formyl(non-limiting example(s) include aldehyde), carboxamido (i.e amido,—C(═O)NH₂), —C(═O)N(alkyl)₂-C(═O)NH(alkyl), —C(═O)N(cycloalkyl)₂,—C(═O)NH(cycloalkyl), alkylC(═O)NH—, -amidino, hydrazido, hydroxamate,—NHC(═O)H, —NHC(═O)alkyl, urea (e.g —NH(C═O)NH₂)—NH(C═O)NH(alkyl),—NH(C═O)NH(alkyl)₂, —NH(C═O)NH(heteroaryl), —NH(C═O)NH(heterocyclyl),guanidinyl, —NHC(═NCN)NH₂, —NHC(═NCN)N(alkyl)₂, carbamoyl (i.e —CO₂NH₂),—NHC(═O)Oalkyl, —CO₂N(alkyl)₂, —NHC(═O)NH—S(O)₂alkyl,—NHC(═O)N(alkyl)₂-S(O)₂alkyl, —NH—S(O)₂alkyl, —NH—S(O)₂heteroaryl,—N(alkyl)-S(O)₂alkyl, —NH—S(O)₂aryl, —N(alkyl)-S(O)₂aryl, —NH—S(O)₂NH₂,—NH—S(O)₂NHalkyl, —NH—S(O)₂N(alkyl)₂, thio, alkylthiocarboxy,—S(O)₂alkyl, —S(O)₂aryl, —OS(O)₂alkyl, —OS(O)₂aryl, sulfonyl urea(non-limiting example(s) include —NHC(═S)NHalkyl) and OSi(alkyl)₃.

“Spiroalkyl” means an alkylene group wherein two carbon atoms of analkyl group are attached to one carbon atom of a parent molecular groupthereby forming a carbocyclic or heterocyclic ring of three to elevenatoms. Representative structures include examples such as:

The spiroalkyl groups of this invention can be optionally substituted byone or more ring system substituents, wherein “ring system substituent”is as defined herein.

“Ring system substituent” also means a cyclic ring of 3 to 7 ring atomsof which may contain 1 or 2 heteroatoms, attached to an aryl,heteroaryl, or heterocyclyl ring by simultaneously substituting two ringhydrogen atoms on said aryl, heteroaryl, heterocyclyl ring. Non-limitingexamples include:

and the like.

The term “optionally substituted” means optional substitution with thespecified groups, radicals or moieties, in available position orpositions.

With reference to the number of moieties (non-limiting example(s)include, substituents, groups or rings) in a compound, unless otherwisedefined, the phrases “one or more” and “at least one” mean that, therecan be as many moieties as chemically permitted, and the determinationof the maximum number of such moieties is well within the knowledge ofthose skilled in the art. Preferably, there are one to threesubstituents, or more preferably, one to two substituents, with at leastone in the para position.

As used herein, the term “composition” is intended to encompass aproduct comprising the specified ingredients in the specified amounts,as well as any product which results, directly or indirectly, fromcombination of the specified ingredients in the specified amounts.

The straight line — as a bond generally indicates a mixture of, oreither of, the possible isomers, non-limiting example(s) include,containing (R)- and (S)-stereochemistry. For example,

A dashed line

represents an optional bond.

Lines drawn into the ring systems, such as, for example:

indicate that the indicated line (bond) may be attached to any of thesubstitutable ring atoms, non limiting examples include carbon, nitrogenand sulfur ring atoms.

As well known in the art, a bond drawn from a particular atom wherein nomoiety is depicted at the terminal end of the bond indicates a methylgroup bound through that bond to the atom, unless stated otherwise. Forexample:

It should also be noted that any heteroatom with unsatisfied valences inthe text, schemes, examples, structural formulae, and any Tables hereinis assumed to have the hydrogen atom or atoms to satisfy the valences.

Prodrugs and solvates of the compounds of the invention are alsocontemplated herein. The term “prodrug”, as employed herein, denotes acompound that is a drug precursor which, upon administration to asubject, undergoes chemical conversion by metabolic or chemicalprocesses to yield a compound of Formula 1 or a salt and/or solvatethereof. A discussion of prodrugs is provided in T. Higuchi and V.Stella, Pro-drugs as Novel Delivery Systems (1987) Volume 14 of theA.C.S. Symposium Series, and in Bioreversible Carriers in Drug Design,(1987) Edward B. Roche, ed., American Pharmaceutical Association andPergamon Press, both of which are incorporated herein by referencethereto.

“Metabolic conjugates”, for example, glucuronides and sulfates which canundergo reversible conversion to compounds of Formula 1 are contemplatedin this application.

“Effective amounts or “therapeutically effective amount” is meant todescribe an amount of compound or a composition of the present inventioneffective to antagonize CXCR3 and thus produce the desired therapeuticeffect in a suitable patient.

“Mammal” means humans and other mammalian animals.

“Patient” includes both human and animals.

“Solvate” means a physical association of a compound of this inventionwith one or more solvent molecules. This physical association involvesvarying degrees of ionic and covalent bonding, including hydrogenbonding. In certain instances the solvate will be capable of isolation,for example when one or more solvent molecules are incorporated in thecrystal lattice of the crystalline solid. “Solvate” encompasses bothsolution-phase and isolatable solvates. Non-limiting examples ofsuitable solvates include ethanolates, methanolates, and the like.“Hydrate” is a solvate wherein the solvent molecule is H₂O. In general,the solvated forms are equivalent to the unsolvated forms and areintended to be encompassed within the scope of this invention.

The compounds of Formula 1 form salts which are also within the scope ofthis invention. Reference to a compound of Formula 1 herein isunderstood to include reference to salts thereof, unless otherwiseindicated. The term “salt(s)”, as employed herein, denotes acidic saltsformed with inorganic and/or organic acids, as well as basic saltsformed with inorganic and/or organic bases. In addition, when a compoundof Formula 1 contains both a basic moiety, such as, but not limited to apyridine or imidazole, and an acidic moiety, such as, but not limited toa carboxylic acid, zwitterions (“inner salts”) may be formed and areincluded within the term “salt(s)” as used herein. Pharmaceuticallyacceptable (non-limiting example(s) include, non-toxic, physiologicallyacceptable) salts are preferred, although other salts are also useful.Salts of the compounds of the Formula 1 may be formed, for example, byreacting a compound of Formula 1 with an amount of acid or base, such asan equivalent amount, in a medium such as one in which the saltprecipitates or in an aqueous medium followed by lyophilization. Acids(and bases) which are generally considered suitable for the formation ofpharmaceutically useful salts from basic (or acidic) pharmaceuticalcompounds are discussed, for example, by S. Berge et al, Journal ofPharmaceutical Sciences (1977) 66(1) 1-19; P. Gould, International J. ofPharmaceutics (1986) 33 201-217; Anderson et al, The Practice ofMedicinal Chemistry (1996), Academic Press, New York; in The Orange Book(Food & Drug Administration, Washington, D.C. on their website); and P.Heinrich Stahl, Camille G. Wermuth (Eds.), Handbook of PharmaceuticalSalts: Properties, Selection, and Use, (2002) Int'l. Union of Pure andApplied Chemistry, pp. 330-331. These disclosures are incorporatedherein by reference thereto.

Exemplary acid addition salts include acetates, adipates, alginates,ascorbates, aspartates, benzoates, benzenesulfonates, bisulfates,borates, butyrates, citrates, camphorates, camphorsulfonates,cyclopentanepropionates, digluconates, dodecylsulfates,ethanesulfonates, fumarates, glucoheptanoates, glycerophosphates,hemisulfates, heptanoates, hexanoates, hydrochlorides, hydrobromides,hydroiodides, 2-hydroxyethanesulfonates, lactates, maleates,methanesulfonates, methyl sulfates, 2-naphthalenesulfonates,nicotinates, nitrates, oxalates, pamoates, pectinates, persulfates,3-phenylpropionates, phosphates, picrates, pivalates, propionates,salicylates, succinates, sulfates, sulfonates (such as those mentionedherein), tartarates, thiocyanates, toluenesulfonates (also known astosylates,) undecanoates, and the like.

Exemplary basic salts include ammonium salts, alkali metal salts such assodium, lithium, and potassium salts, alkaline earth metal salts such ascalcium and magnesium salts, aluminum salts, zinc salts, salts withorganic bases (for example, organic amines) such as benzathines,diethylamine, dicyclohexylamines, hydrabamines (formed withN,N-bis(dehydroabietyl)ethylenediamine), N-methyl-D-glucamines,N-methyl-D-glucamides, t-butyl amines, piperazine,phenylcyclohexylamine, choline, tromethamine, and salts with amino acidssuch as arginine, lysine and the like. Basic nitrogen-containing groupsmay be quarternized with agents such as lower alkyl halides(non-limiting example(s) include methyl, ethyl, propyl, and butylchlorides, bromides and iodides), dialkyl sulfates (non-limitingexample(s) include dimethyl, diethyl, dibutyl, and diamyl sulfates),long chain halides (non-limiting example(s) include decyl, lauryl,myristyl and stearyl chlorides, bromides and iodides), aralkyl halides(non-limiting example(s) include benzyl and phenethyl bromides), andothers.

All such acid salts and base salts are intended to be pharmaceuticallyacceptable salts within the scope of the invention and all acid and basesalts are considered equivalent to the free forms of the correspondingcompounds for purposes of the invention.

Pharmaceutically acceptable esters of the present compounds include thefollowing groups: (1) carboxylic acid esters obtained by esterificationof the hydroxy groups, in which the non-carbonyl moiety of thecarboxylic acid portion of the ester grouping is selected from straightor branched chain alkyl (for example, acetyl, n-propyl, t-butyl, orn-butyl), alkoxyalkyl (for example, methoxymethyl), aralkyl (forexample, benzyl), aryloxyalkyl (for example, phenoxymethyl), aryl (forexample, phenyl optionally substituted with, for example, halogen,C₁₋₄alkyl, or C₁₋₄alkoxy or amino); (2) sulfonate esters, such as alkyl-or aralkylsulfonyl (for example, methanesulfonyl); (3) amino acid esters(for example, L-valyl or L-isoleucyl); (4) phosphonate esters and (5)mono-, di- or triphosphate esters. The phosphate esters may be furtheresterified by, for example, a C₁₋₂₀ alcohol or reactive derivativethereof, or by a 2,3-di(C₆₋₂₄)acyl glycerol.

Compounds of Formula 1, and salts, solvates, esters and prodrugsthereof, may exist in their tautomeric form (for example, as an amide orimino ether). All such tautomeric forms are contemplated herein as partof the present invention.

All stereoisomers (for example, geometric isomers, optical isomers andthe like) of the present compounds (including those of the salts,solvates, esters and prodrugs of the compounds as well as the salts,solvates and esters of the prodrugs), such as those which may exist dueto asymmetric carbons on various substituents, including enantiomericforms (which may exist even in the absence of asymmetric carbons),rotameric forms, atropisomers, and diastereomeric forms, arecontemplated within the scope of this invention. Individualstereoisomers of the compounds of the invention may, for example, besubstantially free of other isomers, or may be admixed, for example, asracemates or with all other, or other selected, stereoisomers. Thechiral centers of the present invention can have the S or Rconfiguration as defined by the IUPAC 1974 Recommendations. The use ofthe terms “salt”, “solvate” “prodrug” and the like, is intended toequally apply to the salt, solvate, ester and prodrug of enantiomers,stereoisomers, rotamers, tautomers, racemates or prodrugs of theinventive compounds.

It should also be noted that throughout the specification and Claimsappended hereto any formula, compound, moiety or chemical illustrationwith unsatisfied valences is assumed to have the hydrogen atom tosatisfy the valences unless the context indicates a bond.

In one embodiment, the present invention discloses compounds of Formula1, having CXCR3 antagonist activity, or a pharmaceutically acceptablederivative thereof, where the various definitions are given above.

In another embodiment of the present invention, Z is N.

In another embodiment, Z is C(H), C(alkyl), C(halogen), C(CF₃) orC(N(R³⁰)₂).

In another embodiment, Z is C(H), C(alkyl), C(F) or C(NH₂).

In another embodiment, G represents a dihydroimidizole, imidazole,dihydrooxazole, oxazole, dihydrooxadiazole, oxadiazole, triazole, ortetrazole ring.

In another embodiment, G is selected from the group consisting of:

wherein

is a single bond or double bond.

In another embodiment, R³ is selected from the group consisting of H,alkyl, haloalkyl, hydroxyalkyl, halogen, —N(R³⁰)₂, —OR³⁰ and —CF₃.

In another embodiment, R³ is selected from the group consisting of H,—CH₃, —CH₂CH₃, cyclopropyl, —F, —Cl, OCH₃, OCF₃ and CF₃.

In another embodiment, R⁴ is selected from the group consisting of H,alkyl, halogen or CF₃.

In another embodiment, R⁶ is selected from the group consisting of H,alkyl, halogen, hydroxyalkyl, —CN, —N(R³)₂, —OR³⁰, —N═CH-alkyl, and—NR³⁰C(═O)alkyl.

In another embodiment, R⁶ is selected from the group consisting of H,—NH₂, —CH₃, —CN and —F.

In another embodiment, R⁸ is selected from the group consisting of H,alkyl, alkenyl, arylalkyl, cycloalkyl, —(CH₂)_(q)OH, —(CH₂)_(q)OR³¹,—(CH₂)_(q)NH₂, —(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹,—(CH₂)_(q)NSO₂R³¹, or —(CH₂)_(q)SO₂NHR³¹.

In another embodiment, R⁹ moieties can be the same or different, eachbeing independently selected from the group consisting of H, alkyl,cycloalkyl, —C(═O)N(H)R³⁰, —C(═O)alkyl, —(CH₂)_(q)OH, —(CH₂)_(q)OR³¹,—(CH₂)_(q)NH₂, —(CH₂)_(q)NHR³¹, —N(H)R³⁰, —N(H)S(O₂)R³¹,—N(H)C(═O)NH(R³⁰), —OR³⁰—SO₂(R³¹), and —SO₂N(H)R³⁰.

In another embodiment, the R⁹ moieties can be the same or different,each being independently selected from the group consisting of H,cyclopropyl, —CF₃, —CH₃, —CH₂OH, —CH₂CH₂OH, —C(CH₃)₂OH, —CH₂CH₂OCH₃,—C(═O)OCH₂CH₃, —CH₂NH₂, —CH₂CH₂NH₂, —CH₂CH₂NHSO₂CH₃, —CH₂CH₂SO₂CH₃,—C(═O)NH₂, —C(═O)N(H)CH₂CH₂OH, —CH₂N(H)C(═O)CF₃, —C(═O)N(H)-cyclopropyl,—C(═O)N(H)CH₂CF₃, —NH₂, —NHCH₃, —N(CH₃)₂, —N(H)CH₂CH₃, —N(H)CH(CH₃)₂,—N(H)CH₂CH₂CH₃, —N(H)CH₂C(═O)OCH₃, —N(H)CH₂CH₂OH, —N(H)CH₂CH₂NH₂,—N(H)CH₂CH₂NHSO₂CH₃, —N(H)CH₂CH₂SO₂CH₃, —N(H)C(═O)N(H)CH₂CH₃,—N(H)CH₂C(═O)NH₂, —OCH₃, ═S and ═O.

In another embodiment, the R⁹ moieties can be the same or different,each being independently selected from the group consisting of H, —CF₃,—CH₃, —CH₂CH₂OH, —CH₂CH₂NH₂, —NH₂, —NHCH₃, —N(H)CH₂CH₃, —N(H)CH(CH₃)₂,—N(H)CH₂CH₂CH₃, —N(H)CH₂C(═O)OCH₃, and —N(H)CH₂CH₂OH.

In another embodiment, R¹⁰ is selected from the group consisting of H,alkyl, aralkyl, hydroxyalkyl, and carbonyl.

In another embodiment, R¹⁰ is selected from the group consisting of—CH₃, —CH₂CH₃ and —CH₂CH₂CH₃, and m is 0-2.

In another embodiment, R¹¹ is selected from the group consisting of H,alkyl, hydroxyalkyl and carbonyl.

In another embodiment, R¹¹ is H or —CH₃.

In another embodiment, R¹² is selected from the group consisting of H,CN, —C(═O)N(R³⁰)₂ and alkyl.

In another embodiment, R¹² is selected from the group consisting of H,—CH₃, CN and —CH₂CH₃.

In another embodiment, the ring atoms of ring D are independently C or Nand substituted by 0-4 R²⁰ moieties.

In another embodiment, ring D is a 5 to 6 membered aryl, heteroaryl,heterocyclenyl, or heterocyclyl ring and substituted by 0-4 R²⁰moieties.

In another embodiment, the R²⁰ moieties can be the same or different,each being independently selected from the group consisting of H, alkyl,alkylaryl, alkynyl, alkoxy, alkylamino, alkylheteroaryl, alkylsulfinyl,alkoxycarbonyl, aminoalkyl, amidinyl, aralkyl, aralkoxy, aryl, aryloxy,cyano, cycloalkyl, cycloalkenyl, halogen, haloalkyl, heteroalkyl,heteroaryl, heterocyclyl, hydroxyalkyl, trifluoromethyl,trifluoromethoxy, —(CH₂)_(q)OR³¹—(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹,—(CH₂)_(q)SO₂R³¹, (CH₂)_(q)NSO₂R³¹, —(CH₂)_(q)SO₂NHR³¹,-alkynylC(R³¹)₂OR³¹, —C(═O)R³⁰, —C(═O)N(R³⁰)₂, —C(═O)OR³⁰, —N(R³⁰)₂,—N(R³⁰)C(═O)R³¹, —NHC(═O)N(R³⁰)₂, —N(R³⁰)C(═O)OR³,—N(R³⁰)C(═NCN)N(R³⁰)₂, —N(R³⁰)C(═O)N(R³⁰)₂, —N(R³⁰)SO₂(R³¹),—N(R³⁰)SO₂N(R³⁰)₂, —OR³⁰, —OC(═O)N(R³⁰)₂, —SR³⁰, —SO₂N(R³⁰)₂—SO₂(R³¹),—OSO₂(R³¹), and —OSi(R³⁰)₃.

In another embodiment, the R²⁰ moieties can be the same or different,each being independently selected from the group consisting of H, alkyl,amino, halogen, CN, CH₃, CF₃, OCF₃, —(CH₂)_(q)OR³, —(CH₂)_(q)NHR³¹,—(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹, —(CH₂)_(q)NSO₂R³¹,—(CH₂)_(q)SO₂NHR³¹, -alkynylC(R³¹)₂OR³¹, —C(═O)R³⁰, —C(═O)OR³⁰,—N(R³⁰)₂, —N(R³⁰)C(═O)R³¹, —NHC(═O)N(R³⁰)₂, —N(R³⁰)C(═O)OR³¹,—N(R³⁰)C(═NCN)N(R³⁰)₂, —N(R³⁰)C(═O)N(R³⁰)₂, —OR³⁰, —OC(═O)N(R³⁰)₂, and—OSO₂(R³¹).

In another embodiment, two R²⁰ moieties are linked together to form afive or six membered aryl, cycloalkyl, heterocyclenyl, heterocyclyl orheteroaryl ring wherein said five or six membered aryl, cycloalkyl,heterocyclenyl, heterocyclyl, and heteroaryl ring is fused to ring D andthe fused ring is optionally substituted with 0 to 4 R²¹ moieties.

In another embodiment, the R²⁰ moieties can be the same or different,each being independently selected from the group consisting of H, —CN,—CH₃, —CF₃, —CH₂OH, —CO₂H, —CO₂CH₃, —NH₂, —NHCH₃, —OCF₃, —OH, F, Cl, Br,—C(═NOH)NH₂, —OCH₂CH₂S(O₂)CH₃, —C(═O)NH₂,

In another embodiment, Y is selected from the group consisting of:—(CHR¹³)_(r)—, —(CR¹³R¹³)_(r)—, —C(═O)— and —CHR¹³C(═O)—.

In another embodiment, Y is selected from the group consisting of:

—CH₂—, —CH(CH₃)—, —CH(CH₂OH)—, —C(═O)— and —CH(CO₂alkyl)-.

In another embodiment, m is 0-2.

In another embodiment, n is 0-2.

In another embodiment, q is 1 or 2.

In another embodiment, r is 1 or 2.

In yet another embodiment:

Z is N, C(H), C(alkyl), C(F) or C(NH₂);

ring G is selected from the group consisting of:

is a single bond or a double bond;

R³ is selected from the group consisting of H, alkyl, haloalkyl,hydroxyalkyl, halogen, —N(R³⁰)₂—OR³⁰ and —CF₃;

R⁶ is selected from the group consisting of H, alkyl, halogen,hydroxyalkyl, —CN, —N(R³⁰)₂, —OR³⁰, —N═CH-alkyl, and —NR³⁰C(═O)alkyl;

R⁹ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, cycloalkyl,—C(═O)N(H)R³⁰, —C(═O)alkyl, —(CH₂)_(q)OH, —(CH₂)_(q)OR³, —(CH₂)_(q)NH₂,—(CH₂)_(q)NHR³, —N(H)R³⁰, —N(H)S(O₂)R³¹, —N(H)C(═O)NH(R³⁰),—OR³⁰—SO₂(R³¹), and —SO₂N(H)R³⁰;

R¹⁰ is selected from the group consisting of H, alkyl, aralkyl,hydroxyalkyl, and carbonyl;

R¹¹ is selected from the group consisting of: H, alkyl, hydroxyalkyl,and carbonyl;

R¹² is selected from the group consisting of H, CN, —C(═O)N(R³⁰)₂ andalkyl;

ring D is a 5 to 6 membered aryl, heteroaryl, heterocyclenyl, orheterocyclyl ring and substituted by 0-4 R²⁰ moieties;

the R²⁰ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, amino, halogen, CN, CH₃,CF₃, OCF₃, —(CH₂)_(q)OR³¹, —(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹,—(CH₂)_(q)SO₂R³¹, —(CH₂)_(q)NSO₂R³¹, —(CH₂)_(q)SO₂NHR³¹,-alkynylC(R³¹)₂OR³¹, —C(═O)R³⁰, —C(═O)OR³⁰, —N(R³⁰)₂, —N(R³⁰)C(═O)R³¹,—NHC(═O)N(R³⁰)₂, —N(R³⁰)C(═O)OR³¹, —N(R³⁰)C(═NCN)N(R³⁰)₂,—N(R³⁰)C(═O)N(R³⁰)₂, —OR³⁰, —OC(═O)N(R³⁰)₂,

Y is selected from the group consisting of: —CH₂—, —CH(CH₃)—,—CH(CH₂OH)—, —C(═O) and —CH(CO₂alkyl)-;

m is 0-2;

n is 0-2;

q is 1 or 2; and

r is 1 or 2.

In still yet another embodiment of the present invention, Formula 1 isrepresented by structural Formula 2, Formula 3, Formula 4, Formula 5,Formula 6 or Formula 7:

or a pharmaceutically acceptable salt, solvate or ester thereof,wherein:

the R⁸ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, alkenyl, alkylaryl,arylalkyl, cycloalkyl, aryl, heteroaryl, heterocyclenyl, heterocyclyl,—(CH₂)_(q)OH, —(CH₂)_(q)OR³¹, —(CH₂)_(q)NH₂, —(CH₂)_(q)NHR³¹,—(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹, —(CH₂)_(q)NSO₂R³¹, or—(CH₂)_(q)SO₂NHR³¹;

the R⁹ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, arylalkyl, alkylaryl,cycloalkyl, heteroaryl, heterocyclenyl, heterocyclyl, —C(═O)N(H)R³⁰,—C(═O)alkyl, —N(H)R³⁰, —N(H)S(O₂)R³¹, —N(H)C(═O)NH(R³⁰), —OR³⁰,—SO₂(R³¹), ═O, ═S, and —SO₂N(H)R³⁰;

L is C or N;

in Formula 4 is a single bond or a double bond; and

m, n, p, q, R¹⁰, R¹¹, R¹², R²⁰ and Y are as defined in claim 1.

In yet another embodiment, in the above shown Formulas 2, 3, 4, 5, 6 and7, R³ is selected from the group consisting of H, alkyl, haloalkyl,hydroxyalkyl, halogen, —N(R³⁰)₂—OR³⁰ and —CF₃.

In yet another embodiment, in the above shown Formulas 2, 3, 4, 5, 6 and7, R⁶ is selected from the group consisting of H, alkyl, halogen,—N(R³⁰)₂, —OR³⁰ and —NR—C(═O)alkyl.

In yet another embodiment, in the above shown Formulas 2, 3, 4, 5, 6 and7, R⁹ moieties are the same or different, each being independentlyselected from the group consisting of H, cyclopropyl, —CF₃, —CH₃,—CH₂CH₃, —CH₂OH, —CH₂CH₂OH, —C(CH₃)₂OH, —CH₂CH₂OCH₃, —C(═O)OCH₂CH₃,—CH₂NH₂, —CH₂CH₂NH₂, —CH₂CH₂NHSO₂CH₃, —CH₂CH₂SO₂CH₃, —C(═O)NH₂,—C(═O)N(H)CH₂CH₂OH, —CH₂N(H)C(═O)CF₃, —C(═O)N(H)-cyclopropyl,—C(═O)N(H)CH₂CF₃, —NH₂, —NHCH₃, —N(CH₃)₂, —N(H)CH₂CH₃, —N(H)CH(CH₃)₂,—N(H)CH₂CH₂CH₃, —N(H)CH₂C(═O)OCH₃, —N(H)CH₂CH₂OH, —N(H)CH₂CH₂NH₂,—N(H)CH₂CH₂NHSO₂CH₃, —N(H)CH₂CH₂SO₂CH₃, —N(H)C(═O)N(H)CH₂CH₃,—N(H)CH₂C(═O)NH₂, ═O, ═S, and —OCH₃.

In yet another embodiment, in the above shown Formulas 2, 3, 4, 5, 6 and7, R¹⁰ is selected from the group consisting of H, alkyl, aralkyl,hydroxyalkyl, and carbonyl.

In yet another embodiment, in the above shown Formulas 2, 3, 4, 5, 6 and7, R¹¹ is selected from the group consisting of: H, alkyl and carbonyl.

In yet another embodiment, in the above shown Formulas 2, 3, 4, 5, 6 and7, R¹² is selected from the group consisting of H, —CH₃, CN or —CH₂CH₃.

In yet another embodiment, in the above shown Formulas 2, 3, 4, 5, 6 and7, the R²⁰ moieties can be the same or different, each beingindependently selected from the group consisting of H, alkyl, amino,halogen, CN, CH₃, CF₃, OCF₃, —(CH₂)_(q)OR³¹, (CH₂)_(q)NHR³¹,—(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³, —(CH₂)_(q)NSO₂R³¹,—(CH₂)_(q)SO₂NHR³¹, -alkynyl C(R³¹)₂OR³¹, —C(═O)R³⁰, —C(═O)OR³⁰,—N(R³⁰)₂, —N(R³⁰)C(═O)R³¹, —NHC(═O)N(R³⁰)₂, —N(R³⁰)C(═O)OR³¹,—N(R³⁰)C(═NCN)N(R³⁰)₂, —N(R³⁰)C(═O)N(R³⁰)₂, —OR³⁰, —OC(═O)N(R³⁰)₂,—OSO₂(R³¹),

In yet another embodiment, in the above-shown Formulas 2, 3, 4, 5, 6 and7, the R²⁰ moieties can be the same or different, each beingindependently selected from the group consisting of H, —CN, —CH₃, —CF₃,—CH₂OH, —CO₂H, —CO₂CH₃, —NH₂, —NHCH₃, —OCF₃, —OH, F, Cl, Br,—C(═NOH)NH₂, —OCH₂CH₂S(O₂)CH₃, —C(═O)NH₂,

In yet another embodiment, in the above-shown Formulas 2, 3, 4, 5, 6 and7, L is carbon.

In yet another embodiment, in the above-shown Formulas 2, 3, 4, 5, 6 and7, L is nitrogen.

In yet another embodiment, in the above-shown Formulas 2, 3, 4, 5, 6 and7, Y is selected from the group consisting of: —CH₂—, —C(═O)—,—CH(CH₂OH)— and —CH(CO₂alkyl)-.

In yet another embodiment, in the above-shown Formulas 2, 3, 4, 5, 6 and7, R³ is selected from the group consisting of H, alkyl, haloalkyl,hydroxyalkyl, halogen, —N(R³⁰)₂, —OR³⁰ and —CF₃;

R⁶ is selected from the group consisting of H, alkyl, halogen, —N(R³⁰)₂,—OR³⁰, and —NR¹C(═O)alkyl;

the R⁹ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, cycloalkyl,—C(═O)N(H)R³⁰, —C(═O)alkyl, —N(H)R³⁰, —N(H)S(O₂)R³¹, —N(H)C(═O)NH(R³⁰),—OR³⁰, —SO₂(R³¹), and —SO₂N(H)R³⁰;

R¹⁰ is selected from the group consisting of H, alkyl, aralkyl,hydroxyalkyl and carbonyl;

the R²⁰ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, amino, halogen, CN, CH₃,CF₃, OCF₃, —(CH₂)_(q)OR³, —(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹,(CH₂)_(q)SO₂R³¹, (CH₂)_(q)NSO₂R³¹, (CH₂)_(q)SO₂NHR³,-alkynylC(R³¹)₂OR³¹, —C(═O)R³⁰, —C(═O)OR³⁰, —N(R³⁰)₂, —N(R³⁰)C(═O)R³¹,—NHC(═O)N(R³⁰)₂, —N(R³⁰)C(═O)OR³¹, —N(R³⁰)C(═NCN)N(R³⁰)₂,—N(R³⁰)C(═O)N(R³⁰)₂, —OR³⁰, —OC(═O)N(R³⁰)₂, and —OSO₂(R³¹),

Y is selected from the group consisting of: —CH₂—, —C(═O)—, —CH(CH₂OH)—and —CH(CO₂alkyl)-;

m is 0-2;

q is 1 or 2; and

r is 1 or 2.

In still another embodiment of the present invention, a compound isselected from the following structures in Table 1 below (orpharmaceutically acceptable salts, solvates or esters thereof) which areshown along with their IC₅₀ ratings. The IC₅₀ values are rated, “A” forIC₅₀ values less than about 25 nanomolar (nM), “B” for IC₅₀ values inthe range of from about 25 to about 100 nM and “C” for IC₅₀ valuesgreater than about 100 nM. For instance, Compound Number 1 has an IC₅₀of 0.2 nM.

TABLE 1 Compound Number STRUCTURE IC₅₀ 1

A 2

A 3

A 4

A 5

A 6

A 7

A 8

A 9

A 10

A 11

A 12

A 13

A 14

A 15

A 16

A 17

A 18

A 19

A 20

A 21

A 22

A 23

A 24

A 25

A 26

A 27

A 28

A 29

A 30

A 31

A 32

A 33

A 34

A 35

A 36

A 37

A 38

A 39

A 40

A 41

A 42

A 43

A 44

A 45

A 46

A 47

A 48

A 49

A 50

A 51

A 52

A 53

A 54

A 55

A 56

A 57

A 58

A 59

A 60

A 61

A 62

A 63

A 64

A 65

A 66

A 67

A 68

A 69

A 70

A 71

A 72

A 73

A 74

A 75

A 76

A 77

A 78

A 79

A 80

A 81

A 82

A 83

A 84

A 85

A 86

A 87

A 88

A 89

A 90

A 91

A 92

A 93

A 94

A 95

A 96

A 97

A 98

A 99

A 100

A 101

A 102

B 103

B 104

B 105

B 106

B 107

B 108

B 109

B 110

B 111

B 112

B 113

B 114

B 115

B 116

B 117

B 118

B 119

B 120

B 121

B 122

B 123

B 124

B 125

B 126

B 127

B 128

B 129

B 130

B 131

B 132

C 133

C 134

C 135

C 136

C 137

C 138

C 139

C 140

C 141

C 142

C 143

C 144

C 145

C 146

C 147

C 148

C 149

C 150

C 151

C 152

C 153

C 154

C 155

C 156

C 157

C 158

C 159

C 160

C 161

C 162

C 163

C 164

C 165

C 166

C 167

C 168

C 169

C 170

C 171

C 172

C 173

C 174

A 175

A

In another embodiment, the compound of Formula 1 is selected from thegroup consisting of:

or a pharmaceutically acceptable salt, solvate or ester thereof. Thehuman IC₅₀ values (in nM) of the above compounds set forth aboveunderneath their chemical structures.

In another embodiment, the compounds of Formula 1 are selected from thegroup consisting of:

or a pharmaceutically acceptable salt, solvate or ester thereof. Thehuman IC₅₀ values (in nM) of the above compounds set forth aboveunderneath their chemical structures.

In yet another aspect, the compound according to Formula 1 can be inpurified form.

In another embodiment, this invention provides a pharmaceuticalcomposition comprising at least one compound of Formula 1, or apharmaceutically acceptable salt, solvate or ester thereof incombination with at least one pharmaceutically acceptable carrier.

In still another embodiment, the invention provides a pharmaceuticalcomposition of Formula 1, further comprising at least one additionalagent, drug, medicament, antibody and/or inhibitor for treating a CXCR3chemokine receptor mediated disease.

When administering a combination therapy to a patient in need of suchadministration, the therapeutic agents in the combination, or apharmaceutical composition or compositions comprising the therapeuticagents, may be administered in any order such as, for example,sequentially, concurrently, together, simultaneously and the like. Theamounts of the various actives in such combination therapy may bedifferent amounts (different dosage amounts) or same amounts (samedosage amounts). Thus, for non-limiting illustration purposes, acompound of Formula III and an additional therapeutic agent may bepresent in fixed amounts (dosage amounts) in a single dosage unit (e.g.,a capsule, a tablet and the like). A commercial example of such singledosage unit containing fixed amounts of two different active compoundsis VYTORIN® (available from Merck Schering-Plough Pharmaceuticals,Kenilworth, N.J.).

In yet another embodiment, the present invention discloses methods forpreparing pharmaceutical compositions comprising the inventiveheterocyclic substituted piperazine compounds of Formula 1 as an activeingredient. In the pharmaceutical compositions and methods of thepresent invention, the active ingredients will typically be administeredin admixture with suitable carrier materials suitably selected withrespect to the intended form of administration, i.e. oral tablets,capsules (either solid-filled, semi-solid filled or liquid filled),powders for constitution, oral gels, elixirs, dispersible granules,syrups, suspensions, and the like, and consistent with conventionalpharmaceutical practices. For example, for oral administration in theform of tablets or capsules, the active drug component may be combinedwith any oral non-toxic pharmaceutically acceptable inert carrier, suchas lactose, starch, sucrose, cellulose, magnesium stearate, dicalciumphosphate, calcium sulfate, talc, mannitol, ethyl alcohol (liquid forms)and the like. Moreover, when desired or needed, suitable binders,lubricants, disintegrating agents and coloring agents may also beincorporated in the mixture. Powders and tablets may be comprised offrom about 5 to about 95 percent inventive composition. Suitable bindersinclude starch, gelatin, natural sugars, corn sweeteners, natural andsynthetic gums such as acacia, sodium alginate, carboxymethylcellulose,polyethylene glycol and waxes. Among the lubricants there may bementioned for use in these dosage forms, boric acid, sodium benzoate,sodium acetate, sodium chloride, and the like. Disintegrants includestarch, methylcellulose, guar gum and the like. Sweetening and flavoringagents and preservatives may also be included where appropriate. Some ofthe terms noted above, namely disintegrants, diluents, lubricants,binders and the like, are discussed in more detail below.

Additionally, the compositions of the present invention may beformulated in sustained release form to provide the rate controlledrelease of any one or more of the components or active ingredients tooptimize the therapeutic effects, i.e. anti-inflammatory activity andthe like. Suitable dosage forms for sustained release include layeredtablets containing layers of varying disintegration rates or controlledrelease polymeric matrices impregnated with the active components andshaped in tablet form or capsules containing such impregnated orencapsulated porous polymeric matrices.

Liquid form preparations include solutions, suspensions and emulsions.As an example may be mentioned water or water-propylene glycol solutionsfor parenteral injections or addition of sweeteners and pacifiers fororal solutions, suspensions and emulsions. Liquid form preparations mayalso include solutions for intranasal administration.

Aerosol preparations suitable for inhalation may include solutions andsolids in powder form, which may be in combination with apharmaceutically acceptable carrier such as inert compressed gas, e.g.nitrogen.

For preparing suppositories, a low melting wax such as a mixture offatty acid glycerides such as cocoa butter is first melted, and theactive ingredient is dispersed homogeneously therein by stirring orsimilar mixing. The molten homogeneous mixture is then poured intoconvenient sized molds, allowed to cool and thereby solidify.

Also included are solid form preparations which are intended to beconverted, shortly before use, to liquid form preparations for eitheroral or parenteral administration. Such liquid forms include solutions,suspensions and emulsions.

The compounds of the invention may also be deliverable transdermally.The transdermal compositions may take the form of creams, lotions,aerosols and/or emulsions and can be included in a transdermal patch ofthe matrix or reservoir type as are conventional in the art for thispurpose.

Preferably the compound is administered orally.

Preferably, the pharmaceutical preparation is in a unit dosage form. Insuch form, the preparation is subdivided into suitably sized unit dosescontaining appropriate quantities of the active components, e.g., aneffective amount to achieve the desired purpose.

The quantity of the inventive active composition in a unit dose ofpreparation may be generally varied or adjusted from about 1.0 milligramto about 1,000 milligrams, preferably from about 1.0 to about 950milligrams, more preferably from about 1.0 to about 500 milligrams, andtypically from about 1 to about 250 milligrams, according to theparticular application. The actual dosage employed may be varieddepending upon the patient's age, sex, weight and severity of thecondition being treated. Such techniques are well known to those skilledin the art.

Generally, the human oral dosage form containing the active ingredientscan be administered 1 or 2 times per day. The amount and frequency ofthe administration will be regulated according to the judgment of theattending clinician. A generally recommended daily dosage regimen fororal administration may range from about 1.0 milligram to about 1,000milligrams per day, in single or divided doses.

Some useful terms are described below:

Capsule—refers to a special container or enclosure made of methylcellulose, polyvinyl alcohols, or denatured gelatins or starch forholding or containing compositions comprising the active ingredients.Hard shell capsules are typically made of blends of relatively high gelstrength bone and pork skin gelatins. The capsule itself may containsmall amounts of dyes, opaquing agents, plasticizers and preservatives.

Tablet—refers to a compressed or molded solid dosage form containing theactive ingredients with suitable diluents. The tablet can be prepared bycompression of mixtures or granulations obtained by wet granulation, drygranulation or by compaction.

Oral gels—refers to the active ingredients dispersed or solubilized in ahydrophillic semi-solid matrix.

Powders for constitution—refers to powder blends containing the activeingredients and suitable diluents which can be suspended in water orjuices.

Diluent—refers to substances that usually make up the major portion ofthe composition or dosage form. Suitable diluents include sugars such aslactose, sucrose, mannitol and sorbitol; starches derived from wheat,corn, rice and potato; and celluloses such as microcrystallinecellulose. The amount of diluent in the composition can range from about10 to about 90% by weight of the total composition, preferably fromabout 25 to about 75%, more preferably from about 30 to about 60% byweight, even more preferably from about 12 to about 60%.

Disintegrants—refers to materials added to the composition to help itbreak apart (disintegrate) and release the medicaments. Suitabledisintegrants include starches; “cold water soluble” modified starchessuch as sodium carboxymethyl starch; natural and synthetic gums such aslocust bean, karaya, guar, tragacanth and agar; cellulose derivativessuch as methylcellulose and sodium carboxymethylcellulose;microcrystalline celluloses and cross-linked microcrystalline cellulosessuch as sodium croscarmellose; alginates such as alginic acid and sodiumalginate; clays such as bentonites; and effervescent mixtures. Theamount of disintegrant in the composition can range from about 2 toabout 15% by weight of the composition, more preferably from about 4 toabout 10% by weight.

Binders—refers to substances that bind or “glue” powders together andmake them cohesive by forming granules, thus serving as the “adhesive”in the formulation. Binders add cohesive strength already available inthe diluent or bulking agent. Suitable binders include sugars such assucrose; starches derived from wheat, corn rice and potato; natural gumssuch as acacia, gelatin and tragacanth; derivatives of seaweed such asalginic acid, sodium alginate and ammonium calcium alginate; cellulosicmaterials such as methylcellulose and sodium carboxymethylcellulose andhydroxypropylmethylcellulose; polyvinylpyrrolidone; and inorganics suchas magnesium aluminum silicate. The amount of binder in the compositioncan range from about 2 to about 20% by weight of the composition, morepreferably from about 3 to about 10% by weight, even more preferablyfrom about 3 to about 6% by weight.

Lubricant—refers to a substance added to the dosage form to enable thetablet, granules, etc. after it has been compressed, to release from themold or die by reducing friction or wear. Suitable lubricants includemetallic stearates such as magnesium stearate, calcium stearate orpotassium stearate; stearic acid; high melting point waxes; and watersoluble lubricants such as sodium chloride, sodium benzoate, sodiumacetate, sodium oleate, polyethylene glycols and d'l-leucine. Lubricantsare usually added at the very last step before compression, since theymust be present on the surfaces of the granules and in between them andthe parts of the tablet press. The amount of lubricant in thecomposition can range from about 0.2 to about 5% by weight of thecomposition, preferably from about 0.5 to about 2%, more preferably fromabout 0.3 to about 1.5% by weight.

Glidents—materials that prevent caking and improve the flowcharacteristics of granulations, so that flow is smooth and uniform.Suitable glidents include silicon dioxide and talc. The amount ofglident in the composition can range from about 0.1% to about 5% byweight of the total composition, preferably from about 0.5 to about 2%by weight.

Coloring agents—excipients that provide coloration to the composition orthe dosage form. Such excipients can include food grade dyes and foodgrade dyes adsorbed onto a suitable adsorbent such as clay or aluminumoxide. The amount of the coloring agent can vary from about 0.1 to about5% by weight of the composition, preferably from about 0.1 to about 1%.

Bioavailability—refers to the rate and extent to which the active drugingredient or therapeutic moiety is absorbed into the systemiccirculation from an administered dosage form as compared to a standardor control. Conventional methods for preparing tablets are known. Suchmethods include dry methods such as direct compression and compressionof granulation produced by compaction, or wet methods or other specialprocedures. Conventional methods for making other forms foradministration such as, for example, capsules, suppositories and thelike are also well known.

It will be apparent to those skilled in the art that many modifications,variations and alterations to the present disclosure, both to materialsand methods, may be practiced. Such modifications, variations andalterations are intended to be within the spirit and scope of thepresent invention.

As stated earlier, the invention includes tautomers, enantiomers andother stereoisomers of the compounds also. Thus, as one skilled in theart knows, certain imidazole compounds may exist in tautomeric forms.Such variations are contemplated to be within the scope of theinvention. Certain compounds of the present invention may exist inmultiple crystalline forms or amorphous forms. All physical forms of thecurrent invention are contemplated.

Compounds of this invention which contain unnatural proportions ofatomic isotopes (i.e. “radiolabeled compounds”) whether their use istherapeutic, diagnostic or as a research reagent are contemplated underthis invention.

Another embodiment of the invention discloses the use of thepharmaceutical compositions disclosed above for treatment of diseases ofa CXCR3 chemokine receptor mediated disease in a patient in need of suchtreatment comprising administering to the patient a therapeuticallyeffective amount of at least one compound according to Formula 1, or apharmaceutically acceptable salt, solvate or ester thereof.

In another embodiment, the method is directed to administering to thepatient (a) an effective amount of at least one compound according toFormula 1, or a pharmaceutically acceptable salt, solvate or esterthereof concurrently or sequentially with (b) at least one additionalagent, drug, medicament, antibody and/or inhibitor for treating a CXCR3chemokine receptor mediated disease, in combination with apharmaceutically acceptable carrier.

In another embodiment, at least one compound of Formula 1 binds to aCXCR3 receptor.

The invention provides methods of preparing compounds of Formula 1, aswell as methods for treating diseases, for example, treatment (e.g.,palliative therapy, curative therapy, prophylactic therapy) of certaindiseases and conditions e.g., inflammatory diseases (e.g., psoriasis,inflammatory bowel disease), autoimmune diseases (e.g., rheumatoidarthritis, multiple sclerosis), graft rejection (e.g., allograftrejection, xenograft rejection), ophthalmic inflammation or dry eye,infectious diseases and tumors. The invention provides a method oftreating a CXCR3 chemokine mediated disease in a patient in need of suchtreatment comprising administering to the patient a therapeuticallyeffective amount of at least one compound of Formula 1, or apharmaceutically acceptable salt, solvate or ester thereof.

The invention provides methods of treating diseases, for example,treatment (e.g., palliative therapy, curative therapy, prophylactictherapy) of certain diseases and conditions such as inflammatorydiseases (e.g., psoriasis, inflammatory bowel disease), autoimmunediseases (e.g., rheumatoid arthritis, multiple sclerosis), graftrejection (e.g., allograft rejection, xenograft rejection), infectiousdiseases as well as cancers and tumors, fixed drug eruptions, cutaneousdelayed-type hypersensitivity responses, ophthalmic inflammation or dryeye, type I diabetes, viral meningitis and tuberculoid leprosycomprising administering: (a) a therapeutically effective amount of atleast one compound according to Formula 1, or a pharmaceuticallyacceptable salt, solvate or ester thereof concurrently or sequentiallywith (b) at least one medicament selected from the group consisting of:disease modifying antirheumatic drugs; nonsteroidal anti-inflammatorydrugs; COX-2 selective inhibitors; COX-1 inhibitors, immunosuppressives(such as cyclosporins and methotrexate); steroids (includingcorticosteroids such as glucorticoids); PDE IV inhibitors, anti-TNF-αcompounds, TNF-α-convertase (TACE) inhibitors, MMP inhibitors, cytokineinhibitors, glucocorticoids, other chemokine inhibitors such as CCR2 andCCR5, CB2-selective inhibitors, p38 inhibitors, biological responsemodifiers; anti-inflammatory agents and therapeutics.

The invention also provides a method of modulating (inhibiting orpromoting) an inflammatory response in an individual in need of suchtherapy. The method comprises administering a therapeutically effectiveamount of a compound (e.g., small organic molecule) which inhibits orpromotes mammalian CXCR3 function in an individual in need thereof. Alsodisclosed is a method of inhibiting or blocking T-cell mediatedchemotaxis in a patient in need of such treatment comprisingadministering to the patient a therapeutically effective amount of acompound of Formula 1 or a pharmaceutically acceptable salt, solvate orester thereof.

Also disclosed is a method of treating inflammatory bowel disease (suchCrohn's disease, ulcerative colitis) in a patient in need of suchtreatment comprising administering to the patient a therapeuticallyeffective amount of at least one compound of Formula 1, or apharmaceutically acceptable salt, solvate or ester thereof.

Also disclosed is a method of treating inflammatory bowel disease in apatient in need of such treatment comprising administering to thepatient a therapeutically effective amount of: (a) at least one compoundof Formula 1, or a pharmaceutically acceptable salt, solvate or esterthereof concurrently or sequentially with (b) at least one compoundselected from the group consisting of: sulfasalazine, 5-aminosalicylicacid, sulfapyridine, anti-TNF compounds, anti-IL-12 compounds,corticosteroids, glucocorticoids, T-cell receptor directed therapies(such as anti-CD3 antibodies), immunosuppressives, methotrexate,azathioprine, and 6-mercaptopurines.

Also disclosed is a method of treating graft rejection in a patient inneed of such treatment comprising administering to the patient atherapeutically effective amount of at least one compound of Formula 1,or a pharmaceutically acceptable salt, solvate or ester thereof.

Also disclosed is a method of treating graft rejection in a patient inneed of such treatment comprising administering to the patient atherapeutically effective amount of: (a) at least one compound ofFormula 1, or a pharmaceutically acceptable salt, solvate or esterthereof concurrently or sequentially with (b) at least one compoundselected from the group consisting of: cyclosporine A, FK-506, FTY720,beta-interferon, rapamycin, mycophenolate, prednisolone, azathioprine,cyclophosphamide and an antilymphocyte globulin.

Also disclosed is a method of treating multiple sclerosis in a patientin need of such treatment the method comprising administering to thepatient a therapeutically effective amount of: (a) a therapeuticallyeffective amount of at least one compound of Formula 1, or apharmaceutically acceptable salt, solvate or ester thereof concurrentlyor sequentially with (b) at least one compound selected from the groupconsisting of: beta-interferon, glatiramer acetate, corticosteroids,glucocorticoids, methotrexate, azathioprine, mitoxantrone, VLA-4inhibitors, FTY720, anti-IL-12 inhibitors, and CB2-selective inhibitors.

Also disclosed is a method of treating multiple sclerosis in a patientin need of such treatment the method comprising administering to thepatient a therapeutically effective amount of: (a) a therapeuticallyeffective amount of at least one compound of Formula 1, or apharmaceutically acceptable salt, solvate or ester thereof concurrentlyor sequentially with (b) at least one compound selected from the groupconsisting of: methotrexate, cyclosporin, leflunomide, sulfasalazine,corticosteroids, β-methasone, β-interferon, glatiramer acetate,prednisone, etonercept, and infliximab.

Also disclosed is a method of treating rheumatoid arthritis in a patientin need of such treatment the method comprising administering to thepatient a therapeutically effective amount of: (a) at least one compoundof Formula 1, or a pharmaceutically acceptable salt, solvate or esterthereof concurrently or sequentially with (b) at least one compoundselected from the group consisting of: non-steroidal anti-inflammatoryagents, COX-2 inhibitors, COX-1 inhibitors, immunosuppressives,cyclosporine, methotrexate, steroids, PDE IV inhibitors, anti-TNF-αcompounds, MMP inhibitors, corticosteroids, glucocorticoids, chemokineinhibitors, CB2-selective inhibitors, caspase (ICE) inhibitors and otherclasses of compounds indicated for the treatment of rheumatoidarthritis.

Also disclosed is a method of treating psoriasis in a patient in need ofsuch treatment the method comprising administering to the patient atherapeutically effective amount of: a) at least one compound of Formula1, or a pharmaceutically acceptable salt, solvate or ester thereofconcurrently or sequentially with (b) at least one compound selectedfrom the group consisting of: immunosuppressives, cyclosporins,methotrexate, steroids, corticosteroids, anti-TNF-α compounds, anti-ILcompounds, anti-IL-23 compounds, vitamin A and D compounds andfumarates.

Also disclosed is a method of treating ophthalmic inflammation(including, for e.g., uveitis, posterior segment intraocularinflammation, Sjogren's syndrome) or dry eye in a patient in need ofsuch treatment the method comprising administering to the patient atherapeutically effective amount of: a) at least one compound accordingto Formula 1, or a pharmaceutically acceptable salt, solvate or esterthereof concurrently or sequentially with (b) at least one compoundselected from the group consisting of: immunosuppressives, cyclosporins,methotrexate, FK506, steroids, corticosteroids, and anti-TNF-αcompounds.

Also disclosed is a method of treating a disease selected from the groupconsisting of: inflammatory disease, rheumatoid arthritis, multiplesclerosis, inflammatory bowel disease, graft rejection, psoriasis, fixeddrug eruptions, cutaneous delayed-type hypersensitivity responses,ophthalmic inflammation (including e.g., uveitis, posterior segmentintraocular inflammation, and Sjogren's syndrome), tuberculoid leprosyand cancer in a patient in need of such treatment, such methodcomprising administering to the patient an effective amount of at leastone compound according to Formula 1, or a pharmaceutically acceptablesalt, solvate or ester thereof.

The invention also provides a method of treating a disease selected fromthe group consisting of: inflammatory disease, rheumatoid arthritis,multiple sclerosis, inflammatory bowel disease, graft rejection,psoriasis, fixed drug eruptions, cutaneous delayed-type hypersensitivityresponses and tuberculoid leprosy, ophthalmic inflammation, type Idiabetes, viral meningitis and cancer in a patient in need of suchtreatment, such method comprising administering to the patient aneffective amount of (a) at least one compound according to Formula 1, ora pharmaceutically acceptable salt, solvate or ester thereofconcurrently or sequentially with (b) at least one medicament selectedfrom the group consisting of: disease modifying antirheumatic drugs;nonsteroidal antiinflammatory drugs; COX-2 selective inhibitors; COX-1inhibitors; immunosuppressives; steroids; PDE IV inhibitors, anti-TNF-αcompounds, MMP inhibitors, corticosteroids, glucocorticoids, chemokineinhibitors, CB2-selective inhibitors, biological response modifiers;anti-inflammatory agents and therapeutics.

Another embodiment of the invention discloses a method of making thesubstituted pyridine compounds, disclosed above.

Unless otherwise stated, the following abbreviations have the statedmeanings in the Examples below:

-   DBU=1,8-diazabicyclo[5.4.0]undec-7-ene-   DBN=1,5-diazabicyclo[4.3.0]non-5-ene-   EDCI=1-(3-dimethylaminopropyl)-3-ethylcarbodiimide-   HATU=N-(Diethylamino)-1H-1,2,3-triazolo[4,5-b]pyridine-1-ylmethylene]-N-methylmethanaminium    Hexafluorophosphate N-oxide-   HOBT=1-hydroxybenzotriazole-   DCC=dicyclohexylcarbodiimide-   Dibal-H=diisobutylaluminum hydride-   DBPD=2-(Di-t-butylphosphino)biphenyl-   DMF=Dimethylformamide-   LAH=lithium aluminum hydride-   NaBH(OAc)₃=sodium triacetoxyborohydride-   NaBH₄=sodium borohydride-   NaBH₃CN=sodium cyanoborohydride-   LDA=lithium diisopropylamide-   p-TsOH=p-toluenesulfonic acid-   p-TsCl=p-toluenesulfonyl chloride-   PPTS=pyridinium p-toluenesulfonate-   m-CPBA=m-Chloroperbenzoic acid-   TMAD=N,N,N′,N′-tetramethylazodicarboxamide-   CSA=camphorsulfonic acid-   NaHMDS=sodium hexamethyl disilylazide-   HRMS=High Resolution Mass Spectrometry-   HPLC=High Performance Liquid Chromatography-   LRMS=Low Resolution Mass Spectrometry-   nM=nanomolar-   Ki=Dissociation Constant for substrate/receptor complex-   pA2=−logEC₅₀, as defined by J. Hey, Eur. J. Pharmacol., (1995), Vol.    294, 329-335.-   Ci/mmol=Curie/mmol (a measure of specific activity)-   Tr=Triphenylmethyl-   Tris=Tris(hydroxymethyl)aminomethane-   THF=Tetrahydrofuran

GENERAL SYNTHESIS

Compounds of the present invention can be prepared by a number of waysevident to one skilled in the art. Preferred methods include, but arenot limited to, the general synthetic procedures described herein. Oneskilled in the art will recognize that one route will be optimaldepending on the choice of appendage substituents. Additionally, oneskilled in the art will recognize that in some cases the order of stepshas to be controlled to avoid functional group incompatibilities. Oneskilled in the art will recognize that a more convergent route (i.e.non-linear or preassembly of certain portions of the molecule) is a moreefficient method of assembly of the target compounds. Methods for thepreparation of compounds of Formula 1 were variables [R¹, R³, R⁴, R⁶,R⁸, R⁹, R¹⁰, R¹¹, R¹², R²⁰, R²¹, Y, A, E, L, Q, Z, m, n, o, w and p] areas defined above, are shown in Schemes 1-4. EN is described below andPr¹, Pr², Pr³ and Pr⁴ are protecting groups exemplified below.

The thus prepared compounds may be analyzed for their composition andpurity as well as characterized by standard analytical techniques suchas, for example, elemental analysis, NMR, mass spectroscopy, and IRspectra.

The starting material and reagents used in preparing compounds describedare either available from commercial suppliers such as Aldrich ChemicalCo. (Wisconsin, USA) and Acros Organics Co. (New Jersey, USA) or wereprepared by literature methods known to those skilled in the art.

-   -   One skilled in the art will recognize that the synthesis of        compounds of Formula 1 may require the need for the protection        of certain functional groups (i.e. derivatization for the        purpose of chemical compatibility with a particular reaction        condition). Suitable protecting groups for carboxylic acids        include methyl, ethyl, isopropyl, or benzyl ester and the like.        Suitable protecting groups for an amine (Pr² or Pr³) include        methyl, benzyl, ethoxyethyl, t-butoxycarbonyl, phthaloyl and the        like. All protecting groups can be appended to and removed by        literature methods known to those skilled in the art.

One skilled in the art will recognize that the synthesis of compounds ofFormula 1 may require the construction of an amide bond. Methods includebut are not limited to the use of a reactive carboxy derivative (e.g.acid halide, or ester at elevated temperatures) or the use of an acidwith a coupling reagent (e.g. DECI, DCC) with an amine at 0° C. to 100°C. Suitable solvents for the reaction are halogenated hydrocarbons,ethereal solvents, dimethylformamide and the like. The reaction may beconducted under pressure or in a sealed vessel.

One skilled in the art will recognize that the synthesis of compounds ofFormula 1 may require the construction of an amine bond. One such methodis but not limited to the reaction of a primary or secondary amine witha reactive carbonyl (e.g. aldehyde or ketone) under reductive aminationconditions. Suitable reducing reagents of the intermediate imine aresodium borohydride, sodium triacetoxyborohydride and the like at 0° C.to 100° C. Suitable solvents for the reaction are halogenatedhydrocarbons, ethereal solvents, dimethylformamide and the like. Anothersuch method is but not limited to the reaction of a primary or secondaryamine with a reactive alkylating agent such as an alkyl halide, benzylhalide, mesylate, tosylate or the like. Suitable solvents for thereaction are halogenated hydrocarbons, ethereal solvents,dimethylformamide and the like. The reaction may be conducted underpressure or in a sealed vessel at 0° C. to 100° C.

One skilled in the art will recognize that the synthesis of compounds ofFormula 1 may require the reduction of a reducible functional group.Suitable reducing reagents include sodium borohydride, lithium aluminumhydride, diborane and the like at −20° C. to 100° C. Suitable solventsfor the reaction are halogenated hydrocarbons, ethereal solvents,dimethylformamide and the like.

One skilled in the art will recognize that the synthesis of compounds ofFormula III may require the oxidation of a functional group. Suitableoxidizing reagents include oxygen, hydrogen peroxide,m-chloroperoxybenzoic acid and the like at −20° C. to 100° C. Suitablesolvents for the reaction are halogenated hydrocarbons, etherealsolvents, water and the like.

The starting materials and the intermediates of a reaction may beisolated and purified if desired using conventional techniques,including but not limited to filtration, distillation, crystallization,chromatography and the like. Such materials can be characterized usingconventional means, including physical constants and spectral data.

GENERAL DESCRIPTION

Step A. Amination of a Pyridine Ring

A suitably protected 2-halo pyridine or phenyl of structure I is reactedwith a piperazine of structure II to form a compound of generalstructure III. Preferably the reaction is carried out in a solvent suchas dioxane or DMF in the presence of a base such as potassium carbonateor cesium carbonate with or without the assistance of a palladiumcatalyst such as palladium acetate. Alternatively, other leaving groupsmay replace the chlorine (O-mesyl, Br etc.) or a group capable ofactivation under the reaction conditions (H, OH, etc.) may be used.

Alternatively, a compound of structure I can be reacted with a compoundof structure XII to form a compound of structure VIII.

Step B.

Optionally, if the product of step A is a protected piperazine ofstructure III, deprotection is required. When Pr² is benzyl orsubstituted benzyl deprotection can be effected by reaction under apressure of hydrogen gas in the presence of a catalyst such aspalladium. When Pr² is ethoxyethyl deprotection can be effected byreaction with trimethylsilyl iodide. When Pr² is t-butoxycarbonyldeprotection can be effected with a strong acid such as trifluoroaceticacid, hydrogen chloride, p-toluenesulfonic acid.

Step C.

A piperazine of structure IV is reacted with a ketone of structure V inthe presence of a reducing agent to form a compound of structure VIwhere R¹² is hydrogen. General conditions for the reductive aminationreaction are described above.

In certain cases Pr³ represents an appropriately substitutedpiperidone-Y-ring D residue.

Step C′ (when R¹²═CN)

A piperazine of structure IV is reacted with a ketone of structure V inthe presence of a reducing agent to form a compound of structure VIwhere R¹² is a cyanide residue. Typical conditions are the reaction ofan equi-molar quantity of a piperazine of structure IV and a ketone ofstructure in the presence of titanium isopropoxide in a halogenatedsolvent such as methylene chloride for 1-48 hours. Subsequent additionof a cyanide source such as dimethylaluminum cyanide affords a compoundof structure VI where R¹² is a cyanide residue.

Step D

A protected piperidine of structure VI or structure X is deprotected toprovide the secondary amine of structure VII or structure XI. When Pr²is benzyl or substituted benzyl deprotection can be effected by reactionunder a pressure of hydrogen gas in the presence of a catalyst such aspalladium. When Pr² is ethoxyethyl deprotection can be effected byreaction with trimethylsilyl iodide. When Pr² is t-butoxycarbonyldeprotection can be effected with a strong acid such as trifluoroaceticacid.

Step D′

Optionally, functional group introduction or manipulation can beperformed as required. A compound of structure VI or structure X, whenR³═Cl or Br is reacted with a organometallic alkylating agent such aalkylboronic acid, or an alkyl halide in the presence of a metal topromote heterocoupling, or nucleophile to yield a different structure ofgeneral structure VII or structure XI where the halogen at the R³position has been replaced by the appropriate group described for R³.

Step E

A secondary piperidine of structure VII or XI is functionalized withring D by methods such as alkylation or acylation to provide compoundsof structure VIII or IX. General methods for such alkylations andacylations are described above and are well known to those skilled inthe art.

Step F

Suitably protected compounds of structure VIII or VI were converted to aheterocycle ring such as imidazole, imidazoline, oxadiazole by either asingle step or multi-step transformations well known to one skilled withthe art. Methods for construction of heterocyclic ring system have beenreviewed in the literature and assembled in compendiums such asComprehensive Heterocyclic Synthesis (Pergamon Press). Specific examplescan be found in the following references: John et al J. Org. Chem.,1982, 47, 2196; Maria et al Synthesis, 2000, 1814; Martin et al J. Med.Chem., 2001, 44, 1561; Morsy et al Pak. J. Sci. Ind. Res, 2000, 43, 208;Koguro et al Synthesis, 1998, 911; Cowden et al Tet. Lett., 2000, 8661;Norton et al Synthesis, 1994, 1406; Carl et al Tet. Lett., 1996, 2935;Gunter et al J. Org. Chem., 1981, 46, 2824. Examples of suchmethodologies are further illustrated in schemes 2-4.

Step F′

Optionally, functional group manipulation of a compound of structure IXmay be done to provide additional related compounds of structure IX.

Compounds of structure IX can be prepared by the general methodsoutlined in scheme 1. Synthesis of the specifically exemplifiedcompounds, were prepared as described in detailed below. The followingEXAMPLES are being provided to further illustrate the present invention.They are for illustrative purposes only; the scope of the invention isnot to be considered limited in any way thereby.

The following examples are intended to illustrate, but not to limit, thescope of the invention.

PREPARATIVE EXAMPLE 1 EN═CO₂Pr¹═CO₂CH₃

Methyl-2,3-dichloro pyridine 5-carboxylate 1 (methyl5,6-dichloronicotinate, BIONET) was prepared from 5,6-Dichloronicotinicacid (ALDRICH), by converting to the acid chloride by treatment withexcess SOCl₂, and refluxed for 1.5 hours followed by methylation inmethanol/pyridine as solvent in nearly quantitative yield. Ref. Musso etal, Bioorg. Med. Chem. Lett., 1997, 7, 1-6.

A round bottomed flask was charged with methyl 2,3-dichloro pyridine5-carboxylate 1 (7 g, 34 mmol), 2-S-ethyl piperazine (prepared as perWilliams et al J. Med. Chem. 1996, 39, 1345,) (75% active, 5.2 g, 34mmol), cesium carbonate (12.15 g, 68 mmol), DBPD (0.74 g, 2.48 mmol),palladium acetate (0.55 g, 2.48 mmol) and 1,4 dioxane (170 ml). Theflask was equipped with a reflux condenser and heated to 80° C. After 36hours the reaction was cooled, diluted with methylene chloride (˜200ml), and washed with water (2×50 ml). The organic layer was dried overanhydrous magnesium sulfate and then concentrated to an oil. The crudeproduct was purified by silica gel chromatography using amethanol/methylene chloride eluent (3% to 10% MeOH) to afford 3 (8.2 g,85%) of the title compound. MS: m/e, M+H=283

PREPARATIVE EXAMPLE 2 EN=Nitrile

2,3-Dichloro 5-cyano pyridine 4 was prepared from 5,6-Dichloronicotinicacid (ALDRICH). The acid was converted to the acid chloride by treatmentwith excess SOCl₂ and refluxed for 1.5 hours. The intermediate acidchloride was reacted with ammonia (aqueous) to get the primary amidewhich on dehydration with excess SOCl₂ at reflux condition afforded 2,3-Dichloro 5-cyano pyridine 4. [Ref. George et al J. Org. Chem, 1979,44, 2697.]

A round bottomed flask was charged with 2,3-Dichloro 5-cyano pyridine 4(20 g, 95.5 mmol), 2-S-ethyl piperazine (prepared as per Williams et alJ. Med. Chem. 1996, 39, 1345) (80% active, 13.7 g, 95.5 mmol), cesiumcarbonate (62.2 g, 191 mmol), DBPD (2.07 g, 6.97 mmol), palladiumacetate (1.56 g, 6.97 mmol) and 1,4 dioxane (475 ml). The flask wasequipped with a reflux condenser and heated to 80° C. under nitrogen.After 48 hours the reaction was cooled, diluted with methylene chloride(˜200 ml), and filtered through celite. The filtrate was concentrated toan oil. The crude product was purified by silica gel chromatographyusing a methanol/methylene chloride eluent (3% to 10% MeOH) to afford 5(18.02 g, 75%) of the title compound.

MS: m/e, M+H=251

PREPARATIVE EXAMPLE 3 EN=Nitrile

A flask was charged 5 (16.3 g, 65.2 mmol), N-Boc piperidine-4-one (16.88g, 84.76 mmol), and 1,2-dichloroethane (170 ml) and was stirred at 60°C. for 20 minutes. The reducing reagent NaB(OAc)₃H (1.5 equivalents) wasadded slowly with stirring. The resulting suspension was allowed to stirat 60° C. for 3 days, then treated with saturated sodium bicarbonatesolution to pH=13, extracted with methylene chloride, and dried overmagnesium sulfate. The solvent was then removed under reduced pressureand the residue was purified by flash chromatography on silica gel using1.5% then 5.0% methanol in methylene chloride as the eluent to provide 7(25.1 g, 89%). MS: m/e, M+H=434.

PREPARATIVE EXAMPLE 4 EN=Ester

A flask was charged with 3 (4 g, 14.1 mmol), N-Boc piperidine-4-one(3.66 g, 18.4 mmol), and 1,2-dichloroethane (40 ml) and was stirred at60° C. for 30 minutes. The reducing reagent NaB(OAc)₃H (1.5 equivalents)was added slowly with stirring. The resulting suspension was allowed tostir at 60° C. for 3 hours. The reaction mixture was diluted withmethylene chloride, then treated with saturated sodium bicarbonatesolution to pH=13, extracted with methylene chloride, and dried overmagnesium sulfate. The solvent was then removed under reduced pressureand the residue was purified by flash chromatography on silica gel using1.0% then 5.0% methanol in methylene chloride as the eluent to provide 8(5.3 g, 81%). MS: m/e, M+H=467

PREPARATIVE EXAMPLE 5 EN=Nitrile

A flask was charged with 5 (1.5 g, 6 mmol), N-benzyl piperidine-4-onederivative 9 (1.59 g, 6.6 mmol), and 1,2-dichloroethane (12 ml) and wasstirred at 60° C. for 30 minutes. The reducing reagent NaB(OAc)₃H (1.5equivalents) was added slowly with stirring. The resulting suspensionwas allowed to stir at room temperature for 48 hours. The reactionmixture was diluted with methylene chloride, then treated with saturatedsodium bicarbonate solution to pH=13, extracted with methylene chloride,and dried over magnesium sulfate. The solvent was then removed underreduced pressure and the residue was purified by flash chromatography onsilica gel using 1.0% then 5.0% methanol in methylene dichloride as theeluent to provide 10 (1.78 g, 62%). MS: m/e, M+H=476

PREPARATIVE EXAMPLE 6 Multi-step Imidazole Formation, EN═CN

To a round bottomed flask charged with amine 11 (2.15 ml, 14.7 mmol) indry toluene (8 ml), solution of trimethyl aluminum in heptane (2M, 7.35ml, 14.7 mmol) was dropped over 15 minutes under nitrogen atmosphere. Tothe reaction mixture a solution of nitrite 10 (4 g, 8.4 mmol) in toluene(32 ml) was added and stirred at room temperature for 24 hours. Thesolvent was removed and the residue was diluted with ethyl acetate,washed with water. The organic layer was dried over magnesium sulfate.The solvent was then removed under reduced pressure and the residue waspurified by flash chromatography on silica gel using 1.0%-5.0% methanolin methylene dichloride with 1.0% aqueous NH₃ as the eluent to providethe amidine intermediate (4.25 g, 83%) MS: m/e, M+H=609. Theintermediate amidine was charged in a 25 ml pear shaped flask withp-TsOH (1.98 g, 10.44 mmol) and melted at 130° C. for 20 hours. Theresidue was redissolved in methylene chloride and washed with saturatedsodium bicarbonate solution. The organic layer was dried over magnesiumsulfate. The solvent was then removed under reduced pressure and theresidue was purified by flash chromatography on silica gel using1.0%-5.0% methanol in methylene dichloride with 1.0% aqueous NH₃ as theeluent to provide the imidazole compound 12, (2.7 g, 75%) MS: m/e,M+H=517.

PREPARATIVE EXAMPLE 7 EN=Nitrile

Compound 7 (1.1 g, 2.53 mmol) was dissolved in ethyl acetate (10 ml) ina 100 ml round-bottomed flask. The resulting solution was treated with 4M HCl in dioxane (5 ml) and allowed to stir at room temperature for 3hours. The solvent was evaporated and the residue was pumped under highvacuum to get the de-protected product 13 as multi-hydrochloride salt(1.2 g, Quantitative). MS: m/e, M+H=334.

PREPARATIVE EXAMPLE 8 Dihydroimidazole Formation, EN═CN

To a round bottomed flask charged with ethylene diamine 14 (2.15 ml,14.7 mmol) in dry toluene (5 ml), solution of trimethyl aluminum inheptane (2M, 5.0 ml, 10 mmol) was dropped over 10 minutes under nitrogenatmosphere. To the reaction mixture a solution of nitrile B (0.87 g, 2.0mmol) in toluene (5 ml) was added and stirred at 70° C. for 24 hours.The solvent was evaporated and the residue was diluted with ethylacetate, washed with water. The organic layer was dried over magnesiumsulfate. The solvent was then removed under reduced pressure and theresidue was purified by flash chromatography on silica gel using1.0%-5.0% methanol in methylene dichloride with 1.0% aqueous NH₃ as theeluent to provide the dihydroimidizole product 15 (0.4 g, 42%). MS: m/e,M+H=477.

PREPARATIVE EXAMPLE 9

Compound 15 (0.39 g, 2.53 mmol) was dissolved in ethyl acetate (10 ml)in a 100 ml round-bottomed flask. The resulting solution was treatedwith 4M HCl in dioxane (10 ml) and allowed to stir at room temperaturefor 16 hours. The solvent was evaporated and the residue was pumpedunder high vacuum to yield a yellow foam of the de-protected product 16as multi-hydrochloride salt (0.44 g, Quant.). MS: m/e, M+H=377.

PREPARATIVE EXAMPLE 10

A round bottomed flask was charged with 16 (50 mg, 70% active amine,0.09 mmol) and triethylamine (0.09 ml, 0.65 mmol) in DMF (2 ml). Thereaction was cooled at −40° C. before 4-chloro benzoyl chloride wasdropped and the reaction mixture was stirred for 15 minutes. Thereaction solution was then diluted with ethyl acetate (100 ml), washedwith saturated sodium bicarbonate (20 ml) and water (20 ml). The organiclayer was dried over magnesium sulfate and concentrated under reducepressure. The residue was purified by flash chromatography on silica gelusing 1.0%-5.0% methanol in methylene dichloride with 1.0% aqueous NH₃as the eluent to provide the dihydroimidizole compound 19 (26 mg, 54%).MS: m/e, M+H=515.

PREPARATIVE EXAMPLE 11

A round bottomed flask was charged with 16 (300 mg, 70% active amine,0.55 mmol) and triethylamine (1.12 ml, 8 mmol) in DMF (4 ml). 4-chlorobenzyl chloride derivative 20 (228 mg, 1.04 mmol) was dropped and thereaction mixture was stirred for 6 hours. The reaction solution was thendiluted with ethyl acetate (100 ml), washed with saturated sodiumbicarbonate (20 ml) and water (20 ml). The organic layer was dried overmagnesium sulfate and concentrated under reduce pressure. The residuewas purified by flash chromatography on silica gel using 1.0%-5.0%methanol in methylene dichloride with 1.0% aqueous NH₃ as the eluent toprovide the dihydroimidizole compound 21 (206 mg, 66%) MS: m/e, M+H=559.

PREPARATIVE EXAMPLE 12

A round bottomed flask was charged with the product of PreparativeExample 11, 21 (115 mg, 0.20 mmol) in THF (4 ml). Lithium borohydridesolution in THF (2M, 0.41 ml, 0.82 mmol) was added at 0° C. and thereaction mixture was stirred at room temperature for 40 hours. Thereaction mixture was then quenched with 5 ml of 1 N HCl and stirred for0.5 hours. Saturated NaOH solution was added to basify and then thereaction was extracted with ethyl acetate. The organic layer was driedover magnesium sulfate and concentrated under reduce pressure. Theresidue was purified by flash chromatography on silica gel using1.0%-5.0% methanol in methylene dichloride with 1.0% aqueous NH₃ as theeluent to provide the 22 (71 mg, 65%) as mixture of diastereomers. Thediastereomers were separated by prep HPLC column using 4.9% methanol inethyl acetate with 0.1% diethylamine as the eluent. MS: m/e, M+H=531.

PREPARATIVE EXAMPLE 13

A round bottomed flask was charged with 16 (100 mg, 70% active amine,0.18 mmol), lithium 2-amino-6-chloronicotinate 23 (57 mg, 0.32 mmol,preparation below), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimidehydrochloride (75 mg, 0.39 mmol), 1-hydroxybenzotriazole (53 mg, 0.39mmol), N,N-diisopropylethylamine (0.5 ml), DMF (5 mL). The resultingsolution was stirred at room temperature for 16 hours. The reactionmixture was diluted with ethyl acetate (100 ml), washed with water (2×20ml). The combined organic layers were dried over magnesium sulfate, andconcentrated in vacuo. The residue was purified by flash chromatographyon silica gel using 1.0%-5.0% methanol in methylene dichloride with 1.0%aqueous NH₃ as the eluent to provide the 24 (27 mg, 27%). MS: m/e,M+H=531.

PREPARATIVE EXAMPLE 14 EN=Nitrile

To a round bottomed flask charged with ethylene diamine 11 (1.4 ml, 9.6mmol) in dry toluene (7 ml), solution of trimethyl aluminum in heptane(2M, 4.81 ml, 9.6 mmol) was dropped over 15 minutes under nitrogenatmosphere (vigorous reaction). To the reaction mixture a solution ofnitrile 7 (2.8 g, 6.4 mmol) in toluene (25 ml) was added and stirred at70° C. for 16 hours. The solvent was removed and the residue was dilutedwith ethyl acetate, washed with water. The organic layer was dried overmagnesium sulfate. The solvent was then removed under reduced pressureand the residue was purified by flash chromatography on silica gel using1.0%-5.0% methanol in methylene dichloride with 1.0% aqueous NH₃ as theeluent to provide the amidine intermediate (2.25 g, 62%). The amidineintermediate was charged in a 25 ml pear shaped flask with p-TsOH (1.1g, 5.82 mmol) and melted at 130° C. for 20 h. The residue redissolved inethyl acetate and washed with saturated sodium bicarbonate solution.Extracted with, 2% MeOH in dichloromethane as the organic layer. Theorganic layer was dried over magnesium sulfate. The solvent was thenremoved under reduced pressure and the residue yielded imidazole 25(1.24 g, 86%).

During the acid mediated cyclization the deprotection of Boc group wasalso achieved. MS: m/e, M+H=375.

PREPARATIVE EXAMPLE 15 Preparation of Compound Number 1 of Table 1

A round bottomed flask was charged with 25 (45 mg, 0.12 mmol), 4-chlorobenzaldehyde (19 mg, 0.13 mmol), and 1,2-dichloroethane (0.6 ml) and wasstirred at 55° C. for 20 minutes. NaB(OAc)₃H (51 mg, 0.24 mmol) wasadded slowly with stirring. The resulting suspension was allowed to stirat room temperature for 3 days, then treated with saturated sodiumbicarbonate solution to pH=13, extracted with methylene chloride, anddried over magnesium sulfate. The solvent was then removed under reducedpressure and the residue was purified by preparative TLC on silica gelusing 5% methanol in methylene chloride as an eluent to afford 26 as afoam (29 mg, 49%). MS: m/e, M+H=499

PREPARATIVE EXAMPLE 16

A round bottomed flask was charged with 25 (150 mg, 0.40 mmol) andtriethylamine (0.17 ml, 1.2 mmol) in DMF (2 ml). Benzyl bromidederivative 27 (88 mg, 0.4 mmol) was dropped and the reaction mixture wasstirred for 48 hours. The reaction solution was then diluted with ethylacetate (100 ml), washed with saturated sodium bicarbonate (20 ml) andwater (20 ml). The organic layer was dried over magnesium sulfate andconcentrated under reduce pressure. The residue was purified by flashchromatography on silica gel using 1.0%-5.0% methanol in methylenedichloride with 1.0% aqueous NH₃ as the eluent to provide 28 (104 mg,50%) as mixture of diastereomers. The diastereomers were partiallyseparated by prep TLC. MS: m/e, M+H=513.

PREPARATIVE EXAMPLE 17

Preparation of compounds of structure 30, was by the same method shownfor Preparative Example 16. MS: m/e, M+H=557.0.

PREPARATIVE EXAMPLE 18

A round bottomed flask was charged with 30 (55 mg, 0.1 mmol) and ammoniain methanol solution (7N, 3 ml, excess) and the reaction mixture wasstirred at 80° C. for 48 hours under sealed conditions. The solvent wasremoved under reduce pressure and the residue was purified by flashchromatography on silica gel using 1.0%-5.0% methanol in methylenedichloride with 1.0% aqueous NH₃ as the eluent to provide 31 (34 mg,64%). MS: m/e, M+H=542.

PREPARATIVE EXAMPLE 19

Preparation of compound 33 was by the same method shown for PreparativeExample 15. MS: m/e, M+H=533.0

PREPARATIVE EXAMPLE 20 EN=Nitrile

Compound 34 (180 mg, 0.9 mmol) was dissolved in DMF (10 ml) followed by35 (304 mg, 0.89 mmol) and potassium carbonate (621 mg, 4.5 mmol). Themixture was heated to 100° C. and stirred for 20 hours. After cooling toroom temperature, most of the solvent was removed in vacuo. Silica gelpurification gave product 36 (142 mg, 30%).

PREPARATIVE EXAMPLE 21 Multi-Step Imidazole Formation, EN=Nitrile

Preparation of compound 37 was by the same method shown for PreparativeExample 6. MS: m/e, M+H=560

PREPARATIVE EXAMPLE 22 Oxadiazole Formation, EN=Ester

A round bottomed flask was charged with 38 (250 mg, 0.5 mmol) andhydrazine hydrate (75 mg, 1.5 mmol) in ethanol (3 ml) and the reactionmixture was stirred at 80° C. for 16 hours. The solvent was removedunder reduced pressure and the residue was purified by flashchromatography on silica gel using 1.0%-5.0% methanol in methylenedichloride with 1.0% aqueous NH₃ as the eluent to provide theintermediate hydrazide (225 mg, 90%). MS: m/e, M+H=509.

The hydrazide intermediate (140 mg, 0.27 mmol) was taken in the solventmixture of chloroform (2.7 ml) and triethyl orthoformate (1 ml) andheated at 70° C. for 16 hours. PPTS (104 mg, 0.41 mmol) was added andthe reaction was stirred for another 4 hours. The solvent was removedunder reduced pressure and the residue was purified by flashchromatography on silica gel using 1.0%-5.0% methanol in methylenedichloride with 1.0% aqueous NH₃ as the eluent to provide oxadiazole 39(88 mg, 62%). MS: m/e, M+H=519.

PREPARATIVE EXAMPLE 23 Triazole Formation, EN═CN

To a round bottomed flask charged with hydrazine monohydrate (45 μl,0.92 mmol) in dry toluene (1 ml), solution of trimethyl aluminum inheptane (2M, 0.92 ml, 1.8 mmol) was dropped over 10 minutes undernitrogen atmosphere. To the reaction mixture a solution of nitrile 10(250 mg, 0.52 mmol) in toluene (2 ml) was added and stirred at 70° C.for 16 hours. The solvent was removed and the residue was diluted withethyl acetate, washed with water. The organic layer was dried overmagnesium sulfate. The solvent was then removed under reduced pressureand the residue was purified by flash chromatography on silica gel using1.0%-5.0% methanol in methylene dichloride with 2.0% aqueous NH₃ as theeluent to provide the amidine intermediate (150 mg, 56%) MS: m/e,M+H=508.

The intermediate amidine (50 mg, 0.1 mmol) was stirred at 70° C. withtriethyl orthoformate (1.98 g, 1 ml) for 2 hours. To the reactionmixture PPTS (37 mg, 0.15 mmol) was added and stirred at 70° C. for 16hours. The solvent was then removed under reduced pressure and theresidue was purified by preparative TLC on silica gel using 5.0%methanol in methylene dichloride with 1.0% aqueous NH₃ as the eluent toprovide the triazole 40 (16 mg, 31%). MS: m/e, M+H=518.

PREPARATIVE EXAMPLE 24 Amino Oxadiazole Formation, EN=Ester

To a round bottomed pressure vessel charged with 8 (600 mg, 1.28 mmol)in methanol (10 ml), hydrazine (411 mg, 12.8 mmol) was added and thereaction mixture was stirred at 70° C. for 19 hours under sealedconditions. The solvent was removed and the residue was diluted withmethylene chloride, washed with water. The organic layer was dried overmagnesium sulfate. The solvent was then removed under reduced pressureto get the intermediate hydrazide (410 mg).

The intermediate hydrazide was redissolved in methylene chloride (1.5ml) and ethyl isocyanate (0.1 ml, 1.5 equivalents) was added. Afterstirring at room temperature for 1 hour, triethylamine (0.35 ml),dimethyl aminopyridine (52 mg) and p-TsCl (195 mg) were added andstirred for 1 day. The reaction was diluted with methylene chloride andwashed with water. The organic layer was dried over magnesium sulfate.The solvent was then removed under reduced pressure and the residue waspurified by flash chromatography on silica gel using 1.0%-5.0% methanolin methylene dichloride as the eluent to provide 41 (120 mg, 18%). MS:m/e, M+H=520.

PREPARATIVE EXAMPLE 25

The oxadiazole 41 (0.12 g, 0.23 mmol) was dissolved in methanol (1.5 ml)in a 100 ml round-bottomed flask. The resulting solution was treatedwith 4M HCl in dioxane (0.3 ml) and allowed to stir at room temperaturefor 7 hours. The solvent was evaporated and the residue was pumped underhigh vacuum to get a yellow foam of the de-protected product as amulti-hydrochloride salt (0.1 g, Quant.). The intermediate was takenalong with lithium 2-amino-6-chloronicotinate (62 mg, 0.34 mmol,preparation below), triethylamine (0.32 ml, 2.3 mmol)) and HATU (131 mg,0.34 mmol) in DMF (3 ml). The resulting solution was stirred at roomtemperature for 12 hours. The reaction mixture was diluted with ethylacetate (100 ml), washed with water (2×20 ml). The combined organiclayers were dried over magnesium sulfate, and concentrated in vacuo. Theresidue was purified by preparative TLC on silica gel using 6.0% 7Nammonia in methanol solution in methylene dichloride as the eluent toprovide 42 (61 mg, 46%). MS: m/e, M+H=574.

PREPARATIVE EXAMPLE 26 Hydantoin Formation, EN═CN

N,O-Dimethylhydroxylamine hydrochloride (125 mg; 1.28 mmol) and ester 43(430 mg; 0.83 mmol) were cooled to −50° C. in 10 ml anhydrous THF.Isopropylmagnesium chloride (1.25 ml of a 2.0M THF solution; 2.48 mmol)was added via syringe over the course of 15 min. After 30 min at −50° C.the reaction was warmed to −10° C. and stirred for another 30 min.Aqueous NH₄Cl (20% wt solution; 10 ml) was added and the reactionmixture was extracted with ethyl acetate. The organic phase was driedover sodium sulfate and concentrated in vacuo to give the Weinreb amide(325 mg; 0.63 mmol) MS: m/e, M+H=520.2. This intermediate was reducedvia DIBAL (0.69 ml of a 1.0M toluene solution; 1.38 mmol) in toluene at−20° C. The reaction was quenched with saturated NaHCO₃, extracted withethyl acetate, dried over sodium sulfate, and concentrated. Silica gelpurification yielded the aldehyde intermediate (170 mg, 54% yield; MS:m/e, M+H=461.3). The aldehyde intermediate (50 mg; 0.1 mmol) was stirredwith NaCN (15 mg; 0.3 mmol) and (NH₄)₂CO₃ (38 mg; 0.4 mmol) in 2 ml of50% aqueous ethanol at 50° C. for 20 h. The product 44 (9 mg) wasdirectly purified via preparative reverse phase chromatography. MS: m/e,M+H=531.2

PREPARATIVE EXAMPLE 27

Preparation of compound 45 was by the same method shown for PreparativeExample 15. MS: m/e, M+H=544.0

PREPARATIVE EXAMPLE 28 Alkylation

Preparation of compound 46 was by the same method shown for PreparativeExample 16. MS: m/e, M+H=591.0.

PREPARATIVE EXAMPLE 29

Preparation of compound 47 was by the same method shown for PreparativeExample 16. MS: m/e, M+H=524.0.

PREPARATIVE EXAMPLE 30

Hydroxylamine hydrochloride (68 mg; 0.96 mmol) and triethylamine (135μl, 0.96 mmol) were taken in ethyl alcohol (2 ml) and stirred for 5 min.Nitrile 47 (250 mg, 0.48 mmol) was added and the reaction mixture wasstirred at 70° C. for 6 hours. The solvent was removed and the residuewas diluted with ethyl acetate and washed with water. The organic phasewas dried over sodium sulfate. The solvent was then removed underreduced pressure and the residue was purified by flash chromatography onsilica gel using 1.0%-5.0% methanol in methylene dichloride with 1.0%aqueous NH₃ as the eluent to provide the product 48 (105 mg, 40%) MS:m/e, M+H=557.

PREPARATIVE EXAMPLE 31

Preparation of compound 49 was by the same method shown for PreparativeExample 11. MS: m/e, M+H=557.0

PREPARATIVE EXAMPLE 32

Preparation of compound 50 was by the same method shown for PreparativeExample 12. MS: m/e, M+H=529.0.

PREPARATIVE EXAMPLE 33

Preparation of compound 51 was by the same method shown for PreparativeExample 11. MS: m/e, M+H=501.0.

PREPARATIVE EXAMPLE 34

Preparation of compound 52 was by the same method shown for PreparativeExample 15. MS: m/e, M+H=551.0.

PREPARATIVE EXAMPLE 35

Preparation of compound 53 was by the same method shown for PreparativeExample 15. MS: m/e, M+H=523.0.

PREPARATIVE EXAMPLE 36

A round bottomed flask was charged with 30 (55 mg, 0.1 mmol) in THF (1ml). The reaction mixture was cooled to 0° C. and methyl magnesiumbromide (0.27 ml, excess) was added. The reaction was stirred at roomtemperature for 16 hours, quenched with ice chips and worked up withethyl acetate and water. The organic phase was dried over sodiumsulfate. The solvent was then removed under reduced pressure and theresidue was purified by flash chromatography on silica gel using1.0%-5.0% methanol in methylene dichloride with 1.0% aqueous NH₃ as theeluent to provide the product 54 (32 mg, 58%). MS: m/e, M+H=557.

PREPARATIVE EXAMPLE 37

A pear shaped flask was charged with 12 (517 mg, 1 mmol) andtrifluoroacetaldehyde ethyl hemiacetal (0.17 ml, 1.5 mmol). The reactionmixture was heated at 120° C. for 6 hours. The residue was purified byflash chromatography on silica gel using 1.0%-5.0% methanol in methylenedichloride with 1.0% aqueous NH₃ as the eluent to provide the product 55(201 mg, 33%). MS: m/e, M+H=615.

PREPARATIVE EXAMPLE 38 Alternate Piperazine Starting Material

Step A

Benzaldehyde (19 mL, 19 g, 0.18 mol) was added to a solution ofD-alanine methyl ester hydrochloride (25 g, 0.18 mol) in dry CH₂Cl₂ (300mL). The solution was stirred at 22° C. for 19 h. The reaction mixturewas cooled with an ice-water bath and solid sodium triacetoxyborohydride(46 g, 0.22 mol) was added in portions over ˜15 min. The cooling bathwas removed and the milky white solution was stirred at 22° C. for 7 h.The solvent was removed by rotary evaporation under reduced pressure andthe resulting slush was partitioned between EtOAc (˜100 mL) and 1 N HCl(˜400 mL). The aqueous layer was extracted with EtOAc (˜50 mL). Theaqueous layer was adjusted to pH ˜10 with 1 N NaOH (450 mL) and themilky aqueous layer was extracted immediately with EtOAc (3×250 mL). Thecombined organic layers were washed with brine (˜250 mL), dried overanhydrous MgSO₄, filtered and concentrated under reduced pressure toafford N-benzyl-D-alanine methyl ester (28 g, 80%) as a colorlesssemi-solid.

Step B.

To a solution of N-benzyl-D-alanine methyl ester (28 g, 0.15 mol) andEDCl.HCl (30.6 g, 0.160 mmol) in CH₂Cl₂ (250 mL) was added a solution ofN-Boc-2(S)-aminobutyric acid (29.5 g, 0.145 mol; Anaspec, Inc.) inCH₂Cl₂ (100 mL). The reaction mixture was stirred at 22° C. for 16 h.Additional N-Boc-2(S)-aminobutyric acid (5.9 g, 29 mmol) and EDCl.HCl(11.1 g, 58 mmol) and DMF (20 mL) were added. After 1 day, the solventswere removed under reduced pressure, and the residue was dissolved inEtOAc. The organic solution was washed with 0.5 N aqueous HCl, saturatedaq. sodium carbonate, brine, and was then dried over anhydrous sodiumsulfate. Subsequent filtration and concentration gave a colorless oil

The oil was dissolved in CH₂Cl₂ (200 mL) and HCl gas was bubbled intothe stirred solution for 1.5 h. After removal of solvent under reducedpressure, the resulting white solid was suspended in EtOAc (500 mL) andaqueous NaHCO₃ solution (150 mL). The mixture was stirred at rt for 18h. The organic layer was separated, washed with brine, dried overanhydrous MgSO₄, filtered, and concentrated to give Compound A35 (21.9g, 61% over 2 steps).

Step C.

The diketopiperazine A35 (21.9 g, 89 mmol) was dissolved in dry THF (500mL). Powdered LiAlH₄ (10.1 g, 267 mmol) was added cautiously and inportions over ˜30 min. The reaction mixture was stirred at 22° C. for 1h, at 65° C. for 1 d, and then at 22° C. for a further 24 h. Thereaction was quenched by cautious dropwise addition of water (10 mL)over 1 h. 1 N aqueous NaOH solution (20 mL) and water (30 mL) were addedsequentially and the milky white reaction mixture was stirred at rt for1 h. The white gelatinous precipitate that formed was removed byfiltration through Celite®. The filter cake was washed copiously withEtOAc (˜500 mL). The combined filtrates were evaporated. The residue wasdissolved in Et₂O (˜500 mL) and then taken to dryness to afford2(S)-ethyl-4-benzyl-5(R)-methylpiperazine (18.4 g, 93%) as a pale goldenyellow oil.

The piperazine above (18.3 g, 84 mmol) was dissolved in CH₂Cl₂ (40 mL)and solid di-t-butyl dicarbonate (18.3 g, 84 mmol) was added. Afterstirring for 30 min at rt, the solvent was removed and the resultingyellow liquid was purified by flash column chromatography, eluting with3:1 hexanes—Et₂O, to afford1-Boc-2(S)-ethyl-4-benzyl-5(R)-methylpiperazine (A36) as a clear,colorless liquid (24.9 g, 93%).

Step D.

A mixture of 1-Boc-2(S)-ethyl-4-benzyl-5(R)-methylpiperazine (A36; 13.6g, 43 mmol), glacial acetic acid (2.5 mL) and 10% Pd/C (4.5 g) inmethanol (150 mL) was shaken under H₂ atmosphere (50 psi) for 24 h. Themixture was filtered through Celite® and the filter cake was washedcopiously with EtOAc (˜500 mL). The combined filtrates were dried overanhydrous MgSO₄, filtered, and concentrated under reduced pressure toafford a clear colorless oil. Further co-evaporation with CH₂Cl₂ (200mL) and Et₂O (2×200 mL) gave the desired1-Boc-2(S)-ethyl-5(R)-methylpiperazine acetic acid salt (A37, 9.7 g) asa viscous oil.

Piperazine A37 may be used in place of piperazine or a substitutedpiperazine in the above examples.

Lithium 2-amino-5-chloronicotinate

A solution of 2,5-dichloronicotinic acid (20.2 g, 0.105 mol) in methanol(500 mL) was cooled to 0° C. and neat thionyl chloride (38 mL, 63 g,0.525 mol) was added over ˜30 min. The reaction mixture was stirred at0° C. for 1 hour. The cooling bath was removed, the reaction temperaturewas allowed to warm to room temperature, and the reaction was allowed tostir for an additional 2 days at room temperature. The solvent wasremoved under reduced pressure to give an off-white residue. The residuewas dissolved in Et₂O (˜500 mL) and the resulting solution was washedsuccessively with saturated aqueous NaHCO₃ solution (˜300 mL), water(˜300 mL), and brine (˜300 mL). The organic layer was separated, driedover anhydrous MgSO₄, and filtered. Removal of the solvent under reducedpressure yielded methyl 2,5-dichloronicotinate (21.0 g, 97%) as a whitesolid.

Performed in duplicate on identical scales in two pressure vessels,methyl 2,5-dichloronicotinate (4.5 g, 22 mmol) was dissolved in ammoniasolution (250 mL, 0.5 M in 1,4-dioxane; 0.125 mol). The pressure vesselswere sealed and heated at (85±5) ° C. for 9 days. The two reactionmixtures were allowed to cool to room temperature, then combined andconcentrated under reduced pressure to yield a white solid. Dissolutionof the solid in 1:1 acetone—MeOH (˜500 mL), followed by adsorption ontosilica gel (25 g) and then purification by flash column chromatography(25:10:1 hexane—CH₂Cl₂—Et₂O), gave 6.08 g (75%) of methyl2-amino-5-chloronicotinate.

A solution of LiOH.H₂O (1.38 g, 33 mmol) in water (33 mL) was added inone portion to a suspension of methyl 2-amino-5-chloronicotinate (6.08g, 27 mmol) in MeOH (110 mL). The reaction mixture was stirred at 70° C.for 24 hours, and gradually became homogeneous. The solvents wereremoved under reduced pressure, and after the resulting white solid wasdried under vacuum (<1 mmHg) to constant weight, 5.51 g (95%) of lithium2-amino-5-chloronicotinate was obtained.

BIOLOGICAL EXAMPLES

The inventive compounds can readily be evaluated to determine activityat The CXCR3 receptors by known methods, such as, for example,Development of Human CXCR3 (N-delta 4) Binding Assay.

Cloning and Expression of Human CXCR3 (N-delta 4):

The DNA encoding human CXCR3 was cloned by PCR using human genomic DNA(Promega, Madison, Wis.) as a template. The PCR primers were designedbased on the published sequence of human orphan receptor GPR9 (1) withincorporated restriction sites, a Kozak consensus sequence, CD8 leaderand Flag tag. The PCR product was subcloned into the mammalianexpression vector pME18Sneo, a derivative of the SR-alpha expressionvector (designated as pME18Sneo-hCXCR3 (N-delta 4).

IL-3-dependent mouse pro-B cells Ba/F3 were transfected byelectroporation in 0.4 ml Dulbecco's PBS containing 4×10⁶ cells with 20μg of pME18Sneo-hCXCR3 (N-delta 4) plasmid DNA. Cells were pulsed at 400Volts, 100 OHMs, 960 μFd. The transfected cells were under selectionwith 1 mg/ml G418 (Life Technologies, Gaithersburg, Md.). G418-resistantBa/F3 clones were screened for CXCR3 expression by specific binding of[¹²⁵I] IP-10 (NEN Life Science Products, Boston, Mass.).

Preparation of Ba/F3-hCXCR3 (N-delta 4) Membranes

Ba/F3 cells expressing human CXCR3 (N-delta 4) were pelleted andresuspended in the lysis buffer containing 10 mM HEPES, pH 7.5 andComplete® protease inhibitors (1 tablet per 100 ml) (BoehringerMannheim, Indianapolis, Ind.) at a cell density of 20×10⁶ cells per ml.After 5 minutes incubation on ice, cells were transferred to 4639 celldisruption bomb (Parr Instrument, Moline, Ill.) and applied with 1,500psi of nitrogen for 30 minutes on ice. Large cellular debris was removedby centrifugation at 1,000×g. Cell membrane in the supernatant wassedimented at 100,000×g. The membrane was resuspended in the lysisbuffer supplemented with 10% sucrose and stored at −80° C. Total proteinconcentration of the membrane was determined by BCA method from Pierce(Rockford, Ill.).

Human CXCR3 (N-delta 4) Scintillation Proximity Assay (SPA)

For each assay point, 2 μg of membrane was preincubated for 1 hr with300 μg wheat germ agglutinin (WGA) coated SPA beads (Amersham, ArlingtonHeights, Ill.) in the binding buffer (50 mM HEPES, 1 mM CaCl₂, 5 mMMgCl₂, 125 mM NaCl, 0.002% NaN₃, 1.0% BSA) at room temperature. Thebeads were spun down, washed once, resuspended in the binding buffer andtransferred to a 96-well Isoplate (Wallac, Gaithersburg, Md.). 25 pM of[¹²⁵I] IP-10 with tested compounds in a series of titration were addedto start the reaction. After 3 hr reaction at room temperature, theamount of [¹²⁵I] IP-10 bound to the SPA beads was determined with aWallac 1450 Microbeta counter.

The IC₅₀ values for the various example compounds of the presentinvention are given in the afore-mentioned Table 1. From these values,it would be apparent to the skilled artisan that the compounds of theinvention have excellent utility CXCR3 antagonists.

While the present invention has been describe in conjunction with thespecific embodiments set forth above, many alternatives, modificationsand variations thereof will be apparent to those of ordinary skill inthe art. All such alternatives, medications and variations are intendedto fall within the spirit and scope of the present invention.

1. A compound having the structure shown in Formula 1

or a pharmaceutically acceptable salt thereof, wherein: Z is C(R²⁹); Grepresents a 5-membered heteroaryl or heterocyclenyl ring containing atleast one —C═N— moiety as part of said heteroaryl or heterocyclenylring, said heteroaryl or heterocyclenyl ring optionally additionallycontaining on the ring one or more moieties which can be the same ordifferent, each being independently selected from the group consistingof N,N(→O), O, S, S(O) and S(O₂), further wherein said heteroaryl orheterocyclenyl ring can be either (i) unsubstituted, or (ii) substitutedon one or more ring carbon atoms with one or more R⁹ substituents, or onone or more ring nitrogen atoms with one or more R⁸ substituents,wherein said R⁸ and R⁹ substituents can be the same or different; R³,R⁴, R⁶ and R²⁹ moieties can be the same or different, each beingindependently selected from the group consisting of H, alkyl, alkylaryl,aralkyl, —CN, CF₃, haloalkyl, cycloalkyl, halogen, hydroxyalkyl,—N═CH—(R³¹), —C(═O)N(R³⁰)₂, —N(R³⁰)₂, —OR³⁰, —SO₂(R³¹),—N(R³⁰)C(═O)N(R³⁰)₂ and —N(R³⁰)C(═)R³¹; the R⁸ moieties can be the sameor different, each being independently selected from the groupconsisting of H, alkyl, alkenyl, alkylaryl, arylalkyl, cycloalkyl, aryl,heteroaryl, heterocyclyl, —(CH₂)_(q)OH, —(CH₂)_(q)OR³¹, —(CH₂)_(q)NH₂,—(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹,—(CH₂)_(q)N(H)SO₂R³¹, —(CH₂)_(q)C(═O)OR³¹, and —(CH₂)_(q)SO₂NHR³¹; theR⁹ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, alkenyl, alkylaryl,arylalkyl, alkoxy, amidinyl, aryl, cycloalkyl, cyano, heteroaryl,heterocyclyl, hydroxyl, —C(═O)N(R³⁰)₂, —C(═S)N(R³⁰)₂, —C(═O)alkyl,—(CH₂)_(q)OH, —(CH₂)_(q)OR³¹, —(CH₂)_(q)NH₂, —(CH₂)_(q)NHR³¹,—(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹, —(CH₂)_(q)N(H)SO₂R³¹,—(CH₂)_(q)SO₂NHR³¹, —N(R³⁰)₂, —N(R³⁰)S(O₂)R³¹, —N(R³⁰)C(═O)N(R³⁰)₂,—OR³⁰, —SO₂(R³¹), —SO₂N(R³⁰)₂, ═O and ═S; the R¹⁰ moieties can be thesame or different, each being independently selected from the groupconsisting of H, alkyl, cycloalkyl, aryl, heteroaryl, heterocyclenyl,heterocyclyl, alkylaryl, arylalkyl, —CO₂H, hydroxyalkyl, —C(═O)N(R³⁰)₂,—(CH₂)_(q)OH, —(CH₂)_(q)OR³¹, —OR³⁰, halogen, ═O, and —C(═O)R³¹; the R¹¹moieties can be the same or different, each being independently selectedfrom the group consisting of H, alkyl, cycloalkyl, aryl, heteroaryl,heterocyclyl, heterocyclenyl, alkylaryl, arylalkyl, carboxamide, CO₂H,—(CH₂)_(q)OH, —(CH₂)_(q)OR³¹, —OR³⁰, halogen, ═O, and —C(═O)R³¹; R¹²moieties can be the same or different, each being independently selectedfrom the group consisting of H, alkyl, —CN, —C(═O)N(R³⁰)₂, —(CH₂)_(q)OH,—(CH₂)_(q)OR³¹ and —S(O₂)R³¹; ring D is a five to nine memberedcycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclenyl orheterocyclyl ring having 0-4 heteroatoms independently selected from O,S or N, wherein ring D is unsubstituted or substituted with 1-5independently selected R²⁰ moieties; the R²⁰ moieties can be the same ordifferent, each being independently selected from the group consistingof H, alkyl, alkenyl, alkylaryl, alkynyl, alkoxy, alkylamino,alkylthiocarboxy, alkylheteroaryl, alkylthio, alkylsulfinyl,alkylsulfonyl, alkoxycarbonyl, aminoalkyl, amidinyl, aralkyl, aralkenyl,aralkoxy, aralkoxycarbonyl, aralkylthio, aryl, aroyl, aryloxy, cyano,cycloalkyl, cycloalkenyl, formyl, guanidinyl, halogen, haloalkyl,heteroaryl, heterocyclyl, heterocyclenyl, hydroxyalkyl, hydroxamate,nitro, trifluoromethoxy, —(CH₂)_(q)OH, —(CH₂)_(q)OR³¹, —(CH₂)_(q)NH₂,—(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹,—(CH₂)_(q)N(H)SO₂R³¹, —(CH₂)_(q),SO₂NHR³¹, -alkynylC(R³¹)₂OR³¹,—C(═O)R³⁰, —C(═O)N(R³⁰)₂, —C(═NR³⁰)NHR³⁰, —C(═NOH)N(R³⁰)₂,—C(═NOR³¹)N(R³⁰)₂, C(═O)OR³⁰, —N(R³⁰)₂, —N(R³⁰)C(═O)R³¹,—NHC(═O)N(R³⁰)₂, —N(R³⁰)C(═O)OR³¹, —N(R³⁰)C(═NCN)N(R³⁰)₂,—N(R³⁰)C(═O)N(R³⁰)SO₂(R³¹), —N(R³⁰)C(═O)N(R³⁰)₂, —N(R³⁰)SO₂(R³¹),—N(R³⁰)S(O)₂N(R³⁰)₂, —OR³⁰, —OC(═O)N(R³⁰)₂, —SR³⁰, —SO₂N(R³⁰)₂,—SO₂(R³¹), —OSO₂(R³¹), and —OSi(R³⁰)₃; or alternatively two R²⁰ moietiesare linked together to form a five or six membered aryl, cycloalkyl,heterocyclyl, heterocyclenyl, or heteroaryl ring wherein said five orsix membered aryl, cycloalkyl, heterocyclyl, heterocyclenyl, orheteroaryl ring is fused to ring D and the fused ring is optionallysubstituted with 0-4 R²¹ moieties; the R²¹ moieties can be the same ordifferent, each being independently selected from the group consistingof H, alkyl, alkenyl, alkylaryl, alkynyl, alkoxy, alkylamino,alkylthiocarboxy, alkylheteroaryl, alkylthio, alkylsulfinyl,alkylsulfonyl, alkoxycarbonyl, aminoalkyl, amidinyl, aralkyl, aralkenyl,aralkoxy, aralkoxycarbonyl, aralkylthio, aryl, aroyl, aryloxy,carboxamido, cyano, cycloalkyl, cycloalkenyl, formyl, guanidinyl,halogen, haloalkyl, heteroaryl, heterocyclyl, heterocyclenyl,hydroxyalkyl, hydroxamate, nitro, trifluoromethoxy, —(CH₂)_(q)OH,—(CH₂)_(q)OR³¹, —(CH₂)_(q)NH₂, —(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹,—(CH₂)_(q)SO₂R³¹, —(CH₂)_(q)N(H)SO₂R³¹, —(CH₂)_(q)SO₂NHR³¹,-alkynylC(R³¹)₂OR³¹, —C(═O)R³⁰, —C(═O)N(R³⁰)₂, —C(═NR³⁰)NHR³⁰,—C(═NOH)N(R³⁰)₂, —C(═NOR³¹)N(R³⁰)₂, —C(═O)OR³⁰, —N(R³⁰)₂,—(R³⁰)C(═O)R³¹, —NHC(═O)N(R³⁰)₂, —N(R³⁰)C(═O)OR³¹,—N(R³⁰)C(═NCN)N(R³⁰)₂, —N(R³⁰)C(═O)N(R³⁰)SO₂(R³¹), —N(R³⁰)C(═O)N(R³⁰)₂,—N(R³⁰)SO₂(R³¹), —(R³⁰)S(O)₂N(R³⁰)₂, —OR³⁰, —OC(═O)N(R³⁰)₂, —SR³⁰,—SO₂N(R³⁰)₂, —SO₂(R³¹), —OSO₂(R³¹), and —Osi(R³⁰)₃; Y is selected fromthe group consisting of —(CR¹³R¹³)_(r)—, —CHR¹³C(═O)—, —(CHR¹³)_(r)O—,—(CHR¹³)_(r)N(R³⁰), —C(═O)—, —C(═NR³⁰)—, —C(═N—OR³⁰)—, —CH(C(═O)NHR³⁰)—,—C(H)(heteroaryl)-, —C(R¹³R¹³)_(r)C)R¹³)═C(R¹³)—, —(CHR¹³)_(r)C(═O)— and—(CHR¹³)_(r)N(H)C(═O)—; or alternatively Y is cycloalkyl,heterocyclenyl, or heterocyclyl wherein the cycloalkyl, heterocyclenyl,or heterocyclyl is fused with ring D; the R¹³ moieties can be the sameor different, each being independently selected from the groupconsisting of H, alkyl, alkylaryl, cycloalkyl, alkoxy, aryl, heteroaryl,heterocyclenyl, heterocyclyl, spiroalkyl, —CN, —CO₂H, —C(═O)R³⁰,—C(═O)N(R³⁰)₂, —(CHR³⁰)_(q)OH, —(CHR³⁰)_(q)OR³¹, —(CHR³⁰)_(q)NH₂, —(CHR³⁰)_(q),NHR³¹, —(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹,—(CH₂)_(q)N(H)SO₂R³¹, —(CH₂)_(q)SO₂NHR³¹, —NH₂, —N(R³⁰)₂,—N(R³⁰)C(═O)N(R³⁰)₂, —N(R³⁰)SO₂(R³¹), —OH, OR³⁰, —SO₂N(R³⁰)₂, and—SO₂(R³¹); the R³⁰ moieties can be the same or different, each beingindependently selected from the group consisting of H, alkyl, alkylaryl,aryl, aralkyl, cycloalkyl, CN, —(CH₂)_(q)OH, —(CH₂)_(q)Oalkyl,—(CH₂)_(q)Oalkylaryl, —(CH₂)_(q)Oaryl, —(CH₂)_(q)Oaralkyl, —(CH₂)_(q),Ocycloalkyl, —(CH₂)_(q)NH₂, —(CH₂)_(q)NHalkyl, —(CH₂)_(q)N(alkyl)₂,—(CH₂)_(q)NHalkylaryl, —(CH₂)_(q)NHaryl, —(CH₂)_(q)NHaralkyl,—(CH₂)_(q)NHcycloalkyl, —(CH₂)_(q)C(═O)NHalkyl,—(CH₂)_(q)C(═O)N(alkyl)₂, —(CH₂)_(q)C(═O)NHalkylaryl,—(CH₂)_(q)C(═O)NHaryl, —(CH₂)_(q)C(═O)NHaralkyl,—(CH₂)_(q)C(═O)NHcycloalkyl, —(CH₂)_(q)SO₂alkyl,—(CH₂)_(q),SO₂alkylaryl, —(CH₂)_(q)SO₂aryl, —(CH₂)_(q)SO₂aralkyl,—(CH₂)_(q)SO₂cycloalkyl, —(CH₂)_(q)N(H)SO₂alkyl—(CH₂)_(q)N(H)SO₂alkylaryl, —(CH₂)_(q)N(H)SO₂aryl,(CH₂)_(q)N(H)SO₂aralkyl —(CH₂)_(q)N(H)SO₂cycloalkyl,—(CH₂)_(q)SO₂NHalkyl, (CH₂)_(q)SO₂NHalkylaryl, (CH₂)_(q)SO₂NHaryl,—(CH₂)_(q)SO₂NHaralkyl, —(CH₂)_(q)SO₂NHcycloalkyl, heterocyclenyl,heterocyclyl, and heteroaryl; the R³¹ moieties can be the same ordifferent, each being independently selected from the group consistingof alkyl, alkylaryl, aryl, aralkyl, cycloalkyl, —(CH₂)_(q)OH,—(CH₂)_(q)Oalkyl, —(CH₂)_(q)Oalkylaryl, —(CH₂)_(q)Oaryl,—(CH₂)_(q)Oaralkyl, —(CH₂)_(q)Ocycloalkyl, —(CH₂)_(q)NH₂,—(CH₂)_(q)NHalkyl, —(CH₂)_(q)N(alkyl)₂, —(CH₂)_(q)NHalkylaryl,—(CH₂)_(q)NHaryl, —(CH₂)_(q)NHaralkyl, —(CH₂)_(q)NHcycloalkyl,—(CH₂)_(q)C(═O)NHalkyl, —(CH₂)_(q)C(═O)N(alkyl)₂,—(CH₂)_(q)C(═O)NHalkylaryl, —(CH₂)_(q)C(═O)NHaryl,—(CH₂)_(q)C(═O)NHaralkyl, —(CH₂)_(q)C(═O)NHcycloalkyl,—(CH₂)_(q)SO₂alkyl, —(CH₂)_(q)SO₂alkylaryl, —(CH₂)_(q)SO₂aryl,—(CH₂)_(q)SO₂aralkyl, —(CH₂)_(q)SO₂cycloalkyl, —CH₂)_(q)N(H)SO₂alkyl—(CH₂)_(q)N(H)SO₂alkylaryl —(CH₂)_(q)N(H)SO₂aryl,—(CH₂)_(q)N(H)SO₂aralkyl, —(CH₂)_(q)N(H)SO₂cycloalkyl,—(CH₂)_(q)SO₂NHalkyl, —(CH₂)_(q)SO₂NHalkylaryl, —(CH₂)_(q)SO₂NHaryl,—(CH₂)_(q)SO₂NHaralkyl, —(CH₂)_(q)SO₂NHcycloalkyl, heterocyclenyl,heterocyclyl, and heteroaryl; m is 0 to 4; n is 0 to 4; each q can bethe same or different, each being independently selected from 1 to 5;and r is 1 to 4; with the proviso that there are no two adjacent doublebonds in any ring, and that when a nitrogen is substituted by two alkylgroups, said two alkyl groups may be optionally joined to each other toform a ring.
 2. The compound according to claim 1, wherein ring G is adihydroimidazole, imidazole, dihydrooxazole, oxazole, dihydrooxadiazole,oxadiazole, dihydrothiazole, thiazole, triazole or tetrazole ring. 3.The compound according to claim 1, wherein Z is C(H), C(alkyl),C(halogen), C(CF₃) or C(N(R³⁰)₂).
 4. The compound according to claim 1,wherein Z is C(alkyl).
 5. The compound according to claim 1, wherein Gis selected from the group consisting of:

wherein

is a single bond or double bond.
 6. The compound according to claim 1,wherein R³ is selected from the group consisting of H, alkyl, haloalkyl,hydroxyalkyl, halogen, —N(R³⁰)₂, —OR³⁰ and —CF₃.
 7. The compoundaccording to claim 6, wherein R³ is selected from the group consistingof H, —CH₃, —CH₂CH₃, cyclopropyl, —F, —Cl, OCH₃, and CF₃.
 8. Thecompound according to claim 1, wherein R⁴ is selected from the groupconsisting of H, alkyl, halogen or CF₃.
 9. The compound according toclaim 1, wherein R⁶ is selected from the group consisting of H, alkyl,halogen, hydroxyalkyl, —CN, —N(R³⁰)₂, —OR³⁰, —N═CH-alkyl, and—NR³⁰C(═O)alkyl.
 10. The compound according to claim 9, wherein R⁶ isselected from the group consisting of H, —NH₂, —CH₃, —CN and —F.
 11. Thecompound according to claim 1, wherein R⁸ is selected from the groupconsisting of H, alkyl, alkenyl, arylalkyl, cycloalkyl, —(CH₂)_(q)OH,—(CH₂)_(q)OR³¹, —(CH₂)_(q)NH₂, —(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹,—(CH₂)_(q)SO₂R³¹, —(CH₂)_(q)N(H)SO₂R³¹, or —(CH₂)_(q),SO₂NHR³¹.
 12. Thecompound according to claim 1, wherein R⁹ moieties can be the same ordifferent, each being independently selected from the group consistingof H, alkyl, cycloalkyl, —C(═O)N(H)R³⁰, —C(═O)alkyl, —(CH₂)_(q)OH,—(CH₂)_(q)OR³¹, —(CH₂)_(q)NH₂, —(CH₂)_(q)NHR³¹, —N(H)R³⁰, —N(H)S(O₂)R³¹,—N(H)C(═O)NH(R³⁰), —OR³⁰, —SO₂(R³¹), and —SO₂N(H)R³⁰.
 13. The compoundaccording to claim 1, wherein the R⁹ moieties can be the same ordifferent, each being independently selected from the group consistingof H, cyclopropyl, —CH₃, —CH₂OH, —CH₂CH₂OH, —CH₂CH₂OCH₃, CH₂OH,—CH₂CH₂NH₂, —CH₂CH₂NHSO₂CH₃, —CH₂CH₂SO₂CH₃, —C(═O)NH₂,—C(═O)N(H)CH₂CH₂OH, C(═O)N(H)-cyclopropyl, NH₂, —NHCH₃, —N(CH₃)₂,—N(H)CH₂CH₃, —N(H)CH(CH₃)₂, —N(H)CH₂CH₂CH₃, —N(H)CH₂CH₂OH,—N(H)CH₂CH₂NH₂, —N(H)CH₂CH₂NHSO₂CH₃, —N(H)CH₂CH₂SO₂CH₃,—N(H)C(═O)N(H)CH₂CH₃, OCH₃, ═S and ═O.
 14. The compound according toclaim 1, wherein R⁹ moieties can be the same or different, each beingindependently selected from the group consisting of H, —CF₃, —CH₃,—CH₂CH₂OH, —CH₂CH₂NH₂, —NH₂, —NHCH₃, —N(H)CH₂CH₃, —N(H)CH(CH₃)₂,—N(H)CH₂CH₂CH₃, and —N(H)CH₂CH₂OH.
 15. The compound according to claim1, wherein R¹⁰ is selected from the group consisting of H, alkyl,aralkyl, hydroxyalkyl, and ═O.
 16. The compound according to claim 15,wherein R¹⁰ is selected from the group consisting of —CH₃, —CH₂CH₃ and—CH₂CH₂CH₃, and m is 0-2.
 17. The compound according to claim 1, whereinR¹¹ is selected from the group consisting of H, alkyl, hydroxyalkyl and═O.
 18. The compound according to claim 17, wherein R¹¹ is H or —CH₃.19. The compound according to claim 1, wherein R¹² is selected from thegroup consisting of H, CN, —C(═O)N(R³⁰)₂ and alkyl.
 20. The compoundaccording to claim 19, wherein R¹² is selected from the group consistingof H, —CH₃, CN and —CH₂CH₃.
 21. The compound according to claim 1,wherein the ring atoms of ring D are independently C or N and whereinring D is substituted by 0-4 R²⁰ moieties.
 22. The compound according toclaim 1, wherein ring D is a 5 to 6 membered aryl, heteroaryl,heterocyclenyl, or heterocyclyl ring and wherein ring D is substitutedby 0-4 R²⁰ moieties.
 23. The compound according to claim 1, wherein theR²⁰ moieties can be the same or different, each being independentlyselected from the group consisting of H, alkyl, alkylaryl, alkynyl,alkoxy, alkylamino, alkylheteroaryl, alkylsulfinyl, alkoxycarbonyl,aminoalkyl, amidinyl, aralkyl, aralkoxy, aryl, aryloxy, cyano,cycloalkyl, cycloalkenyl, halogen, haloalkyl, heteroaryl, heterocyclyl,hydroxyalkyl, trifluoromethyl, trifluoromethoxy, —(CH₂)_(q)OR³¹,—(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹,—(CH₂)_(q)N(H)SO₂R³¹, —(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹,—(CH₂)_(q)N(H)SO₂R³¹, —(CH₂)_(q)SO₂NHR³¹, —alkynylC(R³¹)₂OR³¹,—C(═O)R³⁰, —C(═O)N(R³⁰)₂, —C(═O)OR³⁰, —N(R³⁰)₂, —N(R³⁰)C(═O)R³¹,—NHC(═O)N(R³⁰)₂, —N(R³⁰)C(═O)OR³¹, —N(R³⁰)C(═NCN)N(R³⁰)₂,—N(R³⁰)C(═O)N(R³⁰)₂, —N(R³⁰)SO₂(R³¹), —N(R³⁰)SO₂N(R³⁰)₂,—OR³⁰,)—OC(═O)N(R³⁰)₂, —SR³⁰, —SO₂N(R³⁰)₂, —SO₂(R³¹), —OSO₂(R³¹), and—OSi(R³⁰)₃.
 24. The compound according to claim 1, wherein the R²⁰moieties can be the same or different, each being independently selectedfrom the group consisting of H, alkyl, amino, halogen, CN, CH₃, CF₃,OCF₃, —(CH₂)_(q)OR³¹, —(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹,—(CH₂)_(q)SO₂R³¹, —(CH₂)_(q)N(H)SO₂R³¹, —(CH₂)_(q)SO₂NHR³¹,-alkynylC(R³¹)₂OR³¹, —C(═O)R³⁰, —C(═O)OR³⁰, —N(R³⁰)₂, —N(R³⁰)C(═O)R³¹,—NHC(═O)N(R³⁰)₂, —N(R³⁰)C(═O)OR³¹, —N(R³⁰)C(═NCN)N(R³⁰)₂,—N(R³⁰)C(═O)N(R³⁰)₂, —OR³⁰, —OC(═O)N(R³⁰)₂, and —OSO₂(R³¹).
 25. Thecompound according to claim 1, wherein two R²⁰ moieties are linkedtogether to form a five or six membered aryl, cycloalkyl,heterocyclenyl, heterocyclyl or heteroaryl ring wherein said five or sixmembered aryl, cycloalkyl, heterocyclenyl, heterocyclyl, and heteroarylring is fused to ring D and the fused ring is optionally substitutedwith 0 to 4 R²¹ moieties.
 26. The compound according to claim 1, whereinthe R²⁰ moieties can be the same or different, each being independentlyselected from the group consisting of H, —CN, —CH₃, —CF₃, —CH₂OH, —CO₂H,—CO₂CH₃, —NH₂, —NHCH₃, —OCF₃, —OH, F, Cl, Br, —C(═NOH)NH₂,—OCH₂CH₂S(O₂)CH₃, —C(═O)NH₂,


27. The compound according to claim 1, wherein Y is selected from thegroup consisting of: —(CHR¹³)_(r)—, —(CR¹³R¹³)_(r)—, —C(═O)— and—CHR¹³C(═O)—.
 28. The compound according to claim 1, wherein Y isselected from the group consisting of: —CH₂—, —CH(CH₃)—, —CH(CH₂OH)—,—C(═O)— and CH(CO₂alkyl)-.
 29. The compound according to claim 1,wherein m is 0-2.
 30. The compound according to claim 1, wherein n is0-2.
 31. The compound according to claim 1, wherein q is 1 or
 2. 32. Thecompound according to claim 1, wherein r is 1 or
 2. 33. The compoundaccording to claim 1, wherein ring G is selected from the groupconsisting of:

is a single bond or a double bond; R³ is selected from the groupconsisting of H, alkyl, haloalkyl, hydroxyalkyl, halogen, —N(R³⁰)₂,—OR³⁰ and —CF₃; R⁶ is selected from the group consisting of H, alkyl,halogen, hydroxyalkyl, —CN, —N(R³⁰)₂, —OR³⁰, —N═CH-alkyl, and—NR³OC(═O)alkyl; R⁹ moieties can be the same or different, each beingindependently selected from the group consisting of H, alkyl,cycloalkyl, —C(═O)N(H)R³⁰, —C(═O)alkyl, —(CH₂)_(q)OH, —(CH₂)_(q)OR³¹,—(CH₂)_(q)NH₂, —(CH₂)_(q)NHR³¹, —N(H)R³⁰, —N(H)S(O₂)R³¹,—N(H)C(═O)NH(R³⁰), —OR³⁰ and —SO₂(R³¹); R¹⁰ is selected from the groupconsisting of H, alkyl, hydroxyalkyl, and ═O; R¹¹ is selected from thegroup consisting of: H, alkyl, and ═O; R¹² is selected from the groupconsisting of H, CN, —C(═O)N(R³⁰)₂ and alkyl; ring D is a 5 to 6membered aryl, heteroaryl, heterocyclenyl, or heterocyclyl ring andwherein ring D is substituted by 0-4 R²⁰ moieties; the R²⁰ moieties canbe the same or different, each being independently selected from thegroup consisting of H, alkyl, amino, halogen, CN, CH₃, CF₃, OCF₃,—(CH₂)_(q)OR³¹, —(CH₂)_(q)NHR³¹, —(CH₂)_(q)C(═O)NHR³¹, —(CH₂)_(q)SO₂R³¹,—CH₂)_(q)N(H)SO₂R³¹, —(CH₂)_(q),SO₂NHR³¹, —alkynylC(R³¹)₂OR³¹,—C(═O)R³⁰, —C(═O)OR³⁰, —N(R³⁰)₂, —N(R³⁰)C(═O)R³¹, —NHC(═O)N(R³⁰)₂,—N(R³⁰)C(═O)OR³¹, —N(R³⁰)C(═NCN)N(R³)₂, —N(R³⁰)C(═O)N(R³⁰)₂, —OR³⁰,—OC(═O)N(R³⁰)₂,

Y is selected from the group consisting of: —CH₂—, —CH(CH₃)—,—CH(CH₂OH)—, —C(═O)— and —CH(CO₂alkyl)-; m is 0-2; n is 0-2; and q is 1or
 2. 34. A compound according to claim 1 or a pharmaceuticallyacceptable salt thereof in purified form.
 35. A pharmaceuticalcomposition comprising at least one compound of claim 1, or apharmaceutically acceptable salt thereof, in combination with at leastone pharmaceutically acceptable carrier.
 36. The compound according toclaim 1, selected from the group consisting of: Compound NumberSTRUCTURE 20

24

59

or a pharmaceutically acceptable salt thereof.
 37. A pharmaceuticalcomposition comprising at least one compound of claim 36, or apharmaceutically acceptable salt thereof and at least onepharmaceutically acceptable carrier.